etiology and risk factor of cancer noorwati sutandyo dharmais cancer center / division of...
TRANSCRIPT
![Page 1: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/1.jpg)
Etiology and Risk Factor of Cancer
Noorwati SutandyoDharmais Cancer Center /Dharmais Cancer Center /
Division of Hematology-Medical OncologyDivision of Hematology-Medical OncologyDept Internal MedicineDept Internal Medicine
University of Indonesia School of MedicineUniversity of Indonesia School of Medicine
International Class May 2013
![Page 2: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/2.jpg)
Incidence of cancer is high and going higher every Incidence of cancer is high and going higher every year year Globocan: 12.7 million new cancer cases 2008Globocan: 12.7 million new cancer cases 2008 Nearly Nearly doubledouble to 21.4 million cases by to 21.4 million cases by 20302030
Cancer Cancer causes 1 in 8 deaths causes 1 in 8 deaths worldwide worldwide becoming becoming a global pandemica global pandemic Cancer is killing Cancer is killing moremore people in the developing people in the developing
world world than HIV/AIDS, tuberculosis, and malaria than HIV/AIDS, tuberculosis, and malaria combinedcombined
CANCER CANCER
![Page 3: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/3.jpg)
Jakarta Minimum Cancer Incidence (Coverage 70% )79 Hospitals. 2 Private Clinics, 90 Pathology Laboratories, 44 Municipals Primary health Care (as a coordinator
of 301 Primary Health Care in District area).
![Page 4: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/4.jpg)
Top 10 Malignancy in Dharmais NCC in Male 2005-2007
2.7%
2.9%
3.0%
3.9%
6.3%
7.5%
9.5%
10.1%
13.1%
13.8%
0.0% 2.0% 4.0% 6.0% 8.0% 10.0
%
12.0
%
14.0
%
16.0
%
Soft Tissue
Skin
Prostate Gland
Oral Cavity
Hepar
Leukemia
Lymph Nodes
Colorectum
Pharynx
Bronchus and Lung
Topo
grap
hy
Percent
Top 10 Malignancy in Dharmais NCC
in Female 2005-2007
2.5%
2.8%
2.9%
3.0%
3.2%
3.5%
3.7%
5.6%
17.6%
41.2%
0.0% 10.0% 20.0% 30.0% 40.0% 50.0%
Corpus Uteri
Bronchus and Lung
Pharynx
Leukemia
Lymph Nodes
Thyroid Gland
Colorectum
Ovary
Cervix Uteri
Breast
Topo
grap
hy
Percent
![Page 5: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/5.jpg)
Cancer DefinitionCancer Definition
CCananccer er isis abnormalabnormal growth of growth of cells. cells. Cancer cells Cancer cells will growthwill growth fastfast even with limited of even with limited of
space and nutrition. space and nutrition. Heterogenous:Heterogenous: more than 100 different types of more than 100 different types of
cancercancer Some are Some are familialfamilial : 5-10% : 5-10% (herediter), and others (herediter), and others
are are sporadic sporadic : 90 % : 90 % (non-herediter)(non-herediter)
![Page 6: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/6.jpg)
Tumor = Cancerr???Tumor = Cancerr???
REMEBER: Every REMEBER: Every tumor must be considered tumor must be considered malignant, malignant, until proven malignant/benign until proven malignant/benign
LUMP
Contain: Liquid/Semisolid
Contain: Solid/mass
CYSTS
TUMOR
BENIGN
MALIGNANT
CANCER
![Page 7: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/7.jpg)
Cancer CharacteristicCancer Characteristic
![Page 8: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/8.jpg)
1.Body consist of 1.Body consist of billion cellsbillion cells
2.Inside the cells 2.Inside the cells there is nucleolusthere is nucleolus
3.Inside the 3.Inside the nucleolus there are nucleolus there are
ChromosomChromosom
4.Chomosom 4.Chomosom consist of genesconsist of genes
5.Gene are forms of 5.Gene are forms of DNADNA
![Page 9: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/9.jpg)
DNA-Deoxyribonucleic AcidDNA-Deoxyribonucleic Acid Is Is blue printblue print thatthat contain instruction contain instruction
of orgnism “creation” of orgnism “creation” define human define human characteristic: skin color, eye color, characteristic: skin color, eye color, etc.etc.
DNA consist of DNA consist of nucleotidenucleotide Nucleotide: Nucleotide: sugar+ phosphat + basesugar+ phosphat + base 4 types of base4 types of base: thymine (T), : thymine (T),
adenine (A), guanine (G), and adenine (A), guanine (G), and cytosine (C)cytosine (C)
The fastest computer in the world (2006): IBM Blue Gene/L supercomputer
![Page 10: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/10.jpg)
EverydayEveryday
There are 20.000 DNA damaged There are 20.000 DNA damaged Repaired by DNA repair geneRepaired by DNA repair gene Small part of gene ,can’t be repairedSmall part of gene ,can’t be repaired This is the starting point of cancerThis is the starting point of cancer
![Page 11: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/11.jpg)
CancerCancer
Occur due to Occur due to somatic mutation accumulationsomatic mutation accumulation in in genes that have role in cancer, such as: genes that have role in cancer, such as: OncogenesOncogenes Tumor supressor genesTumor supressor genes Mismatch repair genesMismatch repair genes
CarcinogenesisCarcinogenesis process of the tumor or process of the tumor or neoplasm developmentneoplasm development
Carsinogen Carsinogen The cause of cancerThe cause of cancer
![Page 12: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/12.jpg)
CarsinogenesisCarsinogenesis
Growth promotingGrowth promotingoncogenesoncogenes
Tumor suppressorTumor suppressorgenesgenes
Defect ofGenetic Control
MutationInaktivation
MutationAmplification
DefectDefect
DefectDefect
DNA repairgene
ApoptosisApoptosis
![Page 13: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/13.jpg)
OnkogenesOnkogenes
Type of proto-onkogene mutation:Type of proto-onkogene mutation: point, point, translocation, amplification, insertion and translocation, amplification, insertion and deletiondeletion
Cause cell Cause cell growth or survival growth or survival become dominabecome dominann exceed the activity of other normal genes exceed the activity of other normal genes
Somatic Somatic mutation of proto-onkogenemutation of proto-onkogene:: Occur in various tumor in humanOccur in various tumor in human Occur during carcinogenesis processOccur during carcinogenesis process UUsually, together with other mutations (tumor sually, together with other mutations (tumor
supresor genes and DNA repair genes)supresor genes and DNA repair genes)
![Page 14: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/14.jpg)
Tumor Supressor GenesTumor Supressor Genes
Failed in DNA repairFailed in DNA repair OccurOccur two hits mutations two hits mutations during during
carcinogenesiscarcinogenesis all of gene functions are all of gene functions are diminisheddiminished
p53 protein: p53 protein: guardian of the genomeguardian of the genome Regulation of mitosis cycleRegulation of mitosis cycle Detect and repair DNA damageDetect and repair DNA damage Regulation of apoptosisRegulation of apoptosis
Mutation can be hereditaryMutation can be hereditary
![Page 15: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/15.jpg)
DNA Repair GenesDNA Repair Genes
1. Repair DNA damaged1. Repair DNA damaged
2. If there is 2. If there is Silencing mismatch repair gene Silencing mismatch repair gene cause by cause by somatic DNA methylationsomatic DNA methylation
![Page 16: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/16.jpg)
Cancer Cell DevelopmentCancer Cell Development
Cancer cellCancer cell Comes from one Comes from one
normal normal ‘stem cell’ ‘stem cell’ change tochange to be be a a tumor tumor cell cell graduallygradually
1 cell divide to be 2 – 1 cell divide to be 2 – 4 – and so on different 4 – and so on different one and others one and others showing the showing the cellcell heterogenityheterogenity
![Page 17: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/17.jpg)
![Page 18: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/18.jpg)
Carsinogenesis MultistepCarsinogenesis Multistep
Inisiation:Inisiation: Permanent change in target cell DNAPermanent change in target cell DNA
Promotion:Promotion: Epigenetic change selectivelly influence cell Epigenetic change selectivelly influence cell
proliferation that has done inisiationproliferation that has done inisiation Progression:Progression:
Cell cancer development that shown Cell cancer development that shown autonomy growth, invasive progression, and autonomy growth, invasive progression, and metastasis. metastasis.
![Page 19: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/19.jpg)
![Page 20: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/20.jpg)
Cancer EtiologyCancer Etiology
Several factors that play a Several factors that play a role:role:
•AgeAge•GenetiGeneticc•Hormone Hormone •Immnune systemImmnune system•ObesitasObesitas•Chemical agents Chemical agents (cigarette)(cigarette)•DietDiet•RadiaRadiation tion & UV& UV light light•VirusVirus•StressStress
![Page 21: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/21.jpg)
AgeAge Generally, the risk increasesGenerally, the risk increases in in older personolder person
BUT, cancer can occur to BUT, cancer can occur to anyone, at any age.anyone, at any age.
Tendency, increasing in Tendency, increasing in younger ageyounger age
![Page 22: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/22.jpg)
CarsinogensCarsinogens
Everything causes cancer by causing DNA changes mutagenicmutagenic
Type of carcinogensType of carcinogens Chemical agentsChemical agents VirusVirus RadiationRadiation HormoneHormone NutritionNutrition
![Page 23: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/23.jpg)
CHEMICAL AGENTCHEMICAL AGENT
![Page 24: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/24.jpg)
Chemical CarcinogenChemical Carcinogen
Mostly in forms Mostly in forms pro-carsinogenpro-carsinogen need to need to be be metabolisemetabolise in body to become in body to become activeactive
(( carcinogen carcinogen)) Convert Convert lipophiliclipophilic component component water water
soluble metabolite soluble metabolite (hydrophilic)(hydrophilic) can be can be excreted by urine or bileexcreted by urine or bile
![Page 25: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/25.jpg)
Drugs Metabolism PathwayDrugs Metabolism Pathway
![Page 26: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/26.jpg)
Chemical
Absorption
Distribution
Biotransformation (liver, kidney, lung)
Activation:
Genotoxic
& Non-genotoxic mechanism
InactivationExcretion
(liver, kidney, lung)
Gene Damage
Altered signal transduction
•Hypermutability
•Gene instability
•Loss of proliferation control
•Resistance to apoptosis
CANCER
![Page 27: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/27.jpg)
Chemical CarcinogensChemical CarcinogensGroup Example Cancer
Polycyclic aromatic hydrocarbon
(HPA)
Cigarette smoke, tobacco, grilled meat, smoked meat/fish
Skin, lung, gaster, liver
Aromatic amine and azo dyes
Textile dyes liver, vesica
Nicotine cigarette Lung, oral, respiratory tract
Halogenated compound
Dioxin: heated plastic, PVC, bleaching agents for paper
Kidney, lung, liver
Arsenic Soil, water, plant, cosmetic product, seafood, cigarette
Skin, lung, liver
Nitrosamine Preservatives, coloring agent for meat
Nasopharynx, esophagus, gaster, oral
Alcohol Beverages containing alcohol
Oropharynx, larynx, esophagus, liver, colon, and breast
![Page 28: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/28.jpg)
Chemical carcinogenChemical carcinogen
CigaretteCigarette> 4000 chemical agents> 4000 chemical agents
![Page 29: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/29.jpg)
Chemical Carcinogen Chemical Carcinogen MechanismMechanism
CigaretteCigarette
![Page 30: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/30.jpg)
VIRAL CARCINOGENVIRAL CARCINOGEN
![Page 31: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/31.jpg)
Viral CarcinogenViral Carcinogen Viral oncogenicViral oncogenicDNA and RNADNA and RNA DNA virusDNA virustumor supressor gene inactivation tumor supressor gene inactivation
(p53, Rb)(p53, Rb) HPVHPV 16, 18, 31 16, 18, 31cervical cancercervical cancer EBVEBV Nasopharynx cancer, Burkitt lymphoma, Nasopharynx cancer, Burkitt lymphoma,
Hodgkin DiseaseHodgkin Disease Hepatitis BHepatitis B virus virushepatomahepatoma CMVCMV and herpes and herpes kaposi sacoma (AIDS)kaposi sacoma (AIDS)
RNA virusRNA virus onkogene activationonkogene activation HLTV 1HLTV 1T cell Leukemia, B cell lymphomaT cell Leukemia, B cell lymphoma Hepatitis C Hepatitis C virusvirushepatomahepatoma
![Page 32: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/32.jpg)
Mekanisme Virus DNAMekanisme Virus DNA
DNA virus contain DNA virus contain dsds-DNA -DNA that can be that can be integrated partially or fully integrated partially or fully with with host host chromosomchromosom if it lasts longer, it can give rise to mutations
![Page 33: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/33.jpg)
Oncogenic DNA virus and its Oncogenic DNA virus and its ProductProduct
Virus Gene Product Cell Target
Adenovirus
SV40Polyomavirus
Papillomavirus
E1A E1B
Large T antigen Large T antigen Middle T antigen
E7 E6 E5
Rb p53
Rb, p53 Rb Src, PI3K
Rb p53 PDGF receptor
![Page 34: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/34.jpg)
Spectrum of Cervical Epithelial Changes due to HPV infection
*CIN = cervical intraepithelial neoplasia
Adapted from Goodman A, Wilbur DC. N Engl J Med. 2003;349:1555–1564.
Normal Normal CervixCervix
HPV Infection/HPV Infection/CIN* 1CIN* 1
CIN 2 / CIN 3 /CIN 2 / CIN 3 /Cervical CancerCervical Cancer
![Page 35: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/35.jpg)
Important Function of HPV Important Function of HPV ProteinProtein
Six early Gene (E)Six early Gene (E) regulate mRNA virus synthesis regulate mRNA virus synthesis ans virus genome replicationans virus genome replication
E6E6 & & E7 E7 important in cancer processimportant in cancer process• E6E6 disrupt disrupt supressor tumor p53 supressor tumor p53 proteinprotein• E7E7 inactivate inactivate Retinoblastoma Retinoblastoma proteinprotein
E2E2 suppress E6 & E7 expressionsuppress E6 & E7 expression
Late Gene (L)Late Gene (L) code protein that involved in viral code protein that involved in viral kapsid kapsid assemblyassembly
L1L1 major capsidmajor capsid L2L2 kapsid minorkapsid minor
![Page 36: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/36.jpg)
Cell division cycle keep Cell division cycle keep going with gene mutationgoing with gene mutation
Cycle cell consist of Cycle cell consist of 44 phasephase: :
PhasePhase GGap 1 (ap 1 (preparationpreparation)) Phase Phase SSintesis (DNAintesis (DNA
synthesissynthesis)) PhasePhase GGap 2 (ap 2 (Division Division
preparationpreparation)) Phase Phase MMitosis (itosis (one cell one cell
divide to be 2 cellsdivide to be 2 cells))
Phase Phase GG 0 =0 = resting phase resting phase
Cell Division Cycle
![Page 37: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/37.jpg)
![Page 38: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/38.jpg)
![Page 39: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/39.jpg)
RNA Virus MechanismRNA Virus Mechanism
RNA virus infect cellRNA virus infect cellgenetic material of genetic material of RNA virus become DNA pro-virusRNA virus become DNA pro-virus unite unite with host DNAwith host DNA
Genetic material of RNA can bring part of Genetic material of RNA can bring part of infected host genetic material infected host genetic material v-v-onkogeneonkogene
V-oncogene can be transferred to another cell's genetic material ( (transductiontransduction))
![Page 40: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/40.jpg)
RNA Virus MechanismRNA Virus Mechanism
Oncogenic RNA virus Oncogenic RNA virus create onkogen by:create onkogen by: gettinggetting modificationmodificationCellular gene Cellular gene deregulationderegulation
proto-onkogenproto-onkogen
![Page 41: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/41.jpg)
RADIATION CARCINOGENRADIATION CARCINOGEN
![Page 42: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/42.jpg)
RadiationRadiation
RadiationRadiation Non-ionizingNon-ionizingUVUV IonizingIonizingradio-diagnostic, radio-therapeuticradio-diagnostic, radio-therapeutic
![Page 43: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/43.jpg)
Wave length: 280-320 nm280-320 nmUVB : BCC, SCCUVC: 1 part per million UVClethalUVA: good penetration but poor absorbtion in DNA.
Related with skin cancer kulit Related with skin cancer kulit ((SCC, BCC, and melanoma SCC, BCC, and melanoma malignamaligna))especially in white especially in white peoplepeople
UV RadiationUV Radiation
![Page 44: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/44.jpg)
UV Radiation Carcinogenesis UV Radiation Carcinogenesis MechanismMechanism
CANCER
NORMAL
![Page 45: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/45.jpg)
UV Radiation Carcinogenesis UV Radiation Carcinogenesis MechanismMechanism
CarsinogenesisCarsinogenesis occur if: occur if: P53 mutationP53 mutationcell-cycle arrest not happen, cell-cycle arrest not happen,
disrupt DNA repair disrupt DNA repair excessive proliferationexcessive proliferation Disregulation of pro-apoptosis and anti Disregulation of pro-apoptosis and anti
apoptosisapoptosis apoptosis not happen apoptosis not happenimmortalimmortal
SKIN CANCER
![Page 46: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/46.jpg)
Radiation CarcinogenRadiation Carcinogen Ionizing radiationIonizing radiationradiotherapy, radiotherapy,
radiodiagnosticradiodiagnostic Carsinogenesis mechanismCarsinogenesis mechanism::
Direct cell/macro-molecule damageDirect cell/macro-molecule damage Produce free radicalProduce free radical
Effect:Effect: Enzyme inactivation, Enzyme inactivation, protein changesprotein changes Broken/translocation/point mutation of Broken/translocation/point mutation of
inisiatorinisiator Inhibit cellular immunityInhibit cellular immunitypromotorpromotor
![Page 47: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/47.jpg)
HORMONAL HORMONAL CARCINOGENESISCARCINOGENESIS
![Page 48: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/48.jpg)
HormoneHormone
1. Is proven as a risk factor of several 1. Is proven as a risk factor of several cancer: cancer: breast, endometrium, ovary, breast, endometrium, ovary, prostat, thyroid, testis, bone.prostat, thyroid, testis, bone.
2. Carcinogenesis mechanism of hormone: 2. Carcinogenesis mechanism of hormone: cause cause excessive stimulation of hormone excessive stimulation of hormone to to affected organ affected organ by its receptorby its receptor stimulate stimulate proliferationproliferation
![Page 49: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/49.jpg)
Hormone & Breast CancerHormone & Breast Cancer
Estrogen-2 (Estradiol) :Estrogen-2 (Estradiol) : Has role in Has role in cell growth cell growth and specific organ and specific organ
function.function. More than 100 years ago, it’s been known More than 100 years ago, it’s been known
relation of estrogen and breast cancerrelation of estrogen and breast cancer Estrogen effect is mediated by a protein Estrogen effect is mediated by a protein
that called that called estrogen receptor (ER ).estrogen receptor (ER ).
![Page 50: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/50.jpg)
Estradiol & other steroid hormone stimulate breast cell proliferation facilitate mutation / genetic abnormality
expression
Henderson BE, Bernstein L, Ross R. Etiology of cancer: hormonal factors. In: DeVita VT, Hellman S, Rosenberg SA. Principles & practice of oncology, fifth edition. Philadelphia,2007.
![Page 51: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/51.jpg)
Estrogen Signaling PathwayEstrogen Signaling Pathway Estrogen binds to ER in Estrogen binds to ER in
cytoplasmcytoplasm E-ER complex go to E-ER complex go to
nucleusnucleus Binds with Binds with Estrogen Estrogen
Response ElementResponse Element (ERE) in DNA(ERE) in DNA
It’s called It’s called classic classic pathwaypathway/genomic/ /genomic/ nuclear-initiated steroid nuclear-initiated steroid signaling(NISS)signaling(NISS)
![Page 52: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/52.jpg)
NUTRITION NUTRITION CARCINOGENESISCARCINOGENESIS
![Page 53: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/53.jpg)
Nutrition CarcinogenNutrition Carcinogen Nutrition:Nutrition:
Can be Can be carsinogeniccarsinogenic (negative side)(negative side) Can beCan be inhibitinhibit carsinogenesis, and even can carsinogenesis, and even can
be part of be part of cancer therapy cancer therapy (positive side)(positive side) Carsinogenic and anticarsinogenic of Carsinogenic and anticarsinogenic of
foodfood role in every carcinogenesis step role in every carcinogenesis step
![Page 54: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/54.jpg)
Nutrition CarsinogenNutrition Carsinogen
Nutrients that affect cancer occurrence can be divided into 2 categories :: MicroMicro componentcomponent MacroMacro componen and total caloric intake componen and total caloric intake
Also, can be divided into:Also, can be divided into: GenotoxicGenotoxic agentsagents Non-genotoxic Non-genotoxic agentsagents
![Page 55: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/55.jpg)
GenotoxicGenotoxic Cause Cause DNA damageDNA damage: :
Point mutationsPoint mutations, deletion and insertion, , deletion and insertion, recombination, recombination, rearrangementsrearrangements and and amplification, aberrant chromosomesamplification, aberrant chromosomes
Generally in the form of Generally in the form of micro componentsmicro components Most common: Most common: Heterocyclic aminesHeterocyclic amines (HCA) (HCA)
comes from protein, especially overcooked comes from protein, especially overcooked meat.meat.
![Page 56: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/56.jpg)
Non-genotoxicNon-genotoxic
Carsinogenesis mechanism has not been clearly Carsinogenesis mechanism has not been clearly understandingunderstanding
• Incorporate with genotoxic agents in Incorporate with genotoxic agents in carsinogenesis processcarsinogenesis process
Generally, in the form of Generally, in the form of macro componentsmacro components, , and require higher and longer exposureand require higher and longer exposure
Example: Example: fatfat (breatst cancer and colon cancer), (breatst cancer and colon cancer), Natrium chlorida Natrium chlorida (ca gaster)(ca gaster)
![Page 57: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/57.jpg)
Initiation
Promotion
Progression
DNA Adduct
(DNA + Carcinogen)
Mutation
DNA-repair Normal DNA
Abnormal DNA and cell replication
Precancerous lesion
Invasive lesion
Apoptosis
Promoter
Obesitas
Physical activity
Diet
Intestinal bacterial colonies
Hormone
Growth factor
Immune system
Genotoxic and Nongenotoxic Genotoxic and Nongenotoxic Mechanism Mechanism
Genotoxic
Non-genotoxic
![Page 58: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/58.jpg)
Nutrition CarsinogenNutrition Carsinogen
Other micro componentsOther micro components Alphatoxin B1 Alphatoxin B1 (AFB1) from mold (AFB1) from mold Aspergillus flavus Aspergillus flavus
legumes, corns, soybeans, rice, milk, and cheese HepatomaHepatoma
Hydrazin and agaritin Hydrazin and agaritin compound in undercooeked compound in undercooeked champignon mushroomchampignon mushroom bone carcinoma, gaster, bone carcinoma, gaster, liver, and lung cancerliver, and lung cancer
GlucosideGlucoside in in ferns (ferns (Pterigium sp,.Pterigium sp,. Bracken fern)Bracken fern) vesica, gasterm breast cancervesica, gasterm breast cancer
![Page 59: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/59.jpg)
Nutrition carsinogenNutrition carsinogen
Macro Nutrition:Macro Nutrition: FatFat consumption>> consumption>> positive correlation with positive correlation with
breast, colon, prostate cancer breast, colon, prostate cancer incidenceincidence Fatty acid influence tumorigenesis through Fatty acid influence tumorigenesis through
immune system immune system (eicosanoid metabolite)(eicosanoid metabolite) Saturated fat acids in Saturated fat acids in animal animal andand unsaturatedunsaturated
fatty acids (fatty acids (ΩΩ -6 PUFA) -6 PUFA) from corn oil, from corn oil, sunflower seed oilsunflower seed oil associated with associated with carsinogenesis & tumorigenesiscarsinogenesis & tumorigenesis
![Page 60: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/60.jpg)
SummarySummary
1.1.Cancer is Cancer is a a diseasedisease start from the gene, start from the gene, and end with organ metastases (death)and end with organ metastases (death) and caused by and caused by gene mutationgene mutation
2.2.Genes that play role in cancer are Genes that play role in cancer are oncogenes, tumor suppressor genes, oncogenes, tumor suppressor genes, mismatch repair mismatch repair genesgenes
3.3.The etiology of cancer is called The etiology of cancer is called carsinogencarsinogen, consist of , consist of chemical agents, chemical agents, virus, radiation, hormone, and nutritionvirus, radiation, hormone, and nutrition
![Page 61: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/61.jpg)
4. Some cancer 4. Some cancer can be preventedcan be prevented. . Information about risk factor is important.Information about risk factor is important.
5. Cancer will be an 5. Cancer will be an epidemic diseaseepidemic disease, , every health worker, especially doctors every health worker, especially doctors have to know it better.have to know it better.
![Page 62: Etiology and Risk Factor of Cancer Noorwati Sutandyo Dharmais Cancer Center / Division of Hematology-Medical Oncology Dept Internal Medicine University](https://reader035.vdocuments.site/reader035/viewer/2022062309/5697bfd51a28abf838cad394/html5/thumbnails/62.jpg)