Genetic Predisposition to Cancer COPY

Question 1

What are somatic mutations?

Answer 1

Occur in nongermline tissues

Question 2

What are germline mutations?

Answer 2

Mutations in germ cells - responsible for producing eggs and sperm. Heritable, cause cancer family syndromes

Question 3

What is the function pf proto-oncogenes?

Answer 3

Codes for proteins that regulate cell growth and differentiation

Question 4

What is an oncogene?

Answer 4

Mutated proto-oncogene

Question 5

what is the effect of oncogenes?

Answer 5

Accelerate cell division

Question 6

How many mutations of the chromosomes are needed before control of the cell cycle is lost in oncogenes?

Answer 6

1 mutation needs to occur

Question 7

What is the function of tumour suppressor genes?

Answer 7

Slow down cell divisionRepair DNA mistakesTell cells when to die (a process known as apoptosis or programmed cell death)

Question 8

What is the function of DNA damage response genes?

Answer 8

The repair mechanics for DNACancer arises when both genes fail, speeding the accumulation of mutations in other critical genes

Question 9

What is the function of Mismatch repair genes?

Answer 9

MMR corrects errors that spontaneously occur during DNA replication like single base mismatches or short insertions and deletions

Question 10

What does Micro satellite instability an indicator of?

Answer 10

Phenotypic evidence that MMR is not functioning normally. Cells with abnormally functioning MMR tend to accumulate errors, simple sequence repeats are created

Question 11

Give an example of a cancer syndrome associated with Oncogenes

Answer 11

MEN2 (Multiple endocrine neoplasia)Familial medullary thyroid cancerCan be caused by viruses

Question 12

Give an example of a cancer syndrome associated with Tumour suppressor gene

Answer 12

Breast/ovarian cancer FAP Li-Fraumeni syndrome Retinoblastoma

Question 13

Give an example of a cancer syndrome associated with DNA repair (mis-match repair)

Answer 13

HNPCC / Lynch Syndrome (Hereditary non-polyposis colon cancer)

Question 14

What are other causes of cancer?

Answer 14

Autosomal recessive syndromesE.g. MYH polyposisMultiple modifier genes of lower genetic risk

Question 15

What is a De Novo mutation?

Answer 15

New (de novo) mutation occurs in germ cell of parentNo family history of hereditary cancer syndromeA new mutation in a germ cell?

Question 16

Describe cancer susceptibility genes

Answer 16

They are dominant with incomplete penetrance

Question 17

Is heritable retinoblastoma usually bilateral or unilateral?

Answer 17

Usually bilateral

Question 18

Does heritable retinoblastoma usually contain a family history?

Answer 18

Yes in 20 percent of cases

Question 19

What are the risk factors of breast cancer?

Answer 19

Ageing, family history, Early menarche - first period, late menopause, Nulliparity -not having childrenEstrogen use, dietary factors, lack of exercise.

Question 20

What are the common genes responsible for breast cancer?

Answer 20

BRCA1BRCA2TP53PTENUndiscovered genes

Question 21

What is the function of BRCA1?

Answer 21

Checkpoint mediatorDNA damage signalling and repairChromatin remodelling (inactive X chromosome)Transcription (not essential for this)(PROTEIN THAT ACTS AS A TUMOUR SUPPRESSOR)

Question 22

What is the function of BRCA2?

Answer 22

DNA repair by HR (homologous recombination)

Question 23

What are the BRCA1 associated cancers?

Answer 23

Breast cancers, second primary breast cancerOvarian cancer

Question 24

What are the BRCA2 associated cancers?

Answer 24

Breast cancer, ovarian cancer, male breast cancerIncreased risk of prostate, laryngeal, and pancreatic cancers (magnitude unknown)

Question 25

What are risk factors for colorectal cancers?

Answer 25

AgeingPersonal history of CRC or adenomasHigh-fat, low-fibre dietInflammatory bowel diseaseFamily history of CRC

Question 26

What is the sequence of events for Adenoma to carcinoma?

Answer 26

Epithelium becomes hyperactive, adenoma forms, carcinoma forms

Question 27

How many adenomas are present in non-polyposis (Hereditary Colorectal Cancer (CRC) syndromes)

Answer 27

few to no adenomasHNPCC (hereditary non-polyposis colon cancer / Lynch Syndrome) - CRC &/or endometrial cancer (EC

Question 28

How many adenomas are present in polyposis (Hereditary Colorectal Cancer (CRC) syndromes)

Answer 28

(multiple adenomas)FAP – severe colonic polyposis +/- CRC AFAP - less severe colonic polyposis +/- CRC MAP – varying degrees of colonic polyposis +/- CRCFAP – familial adenomatous polyposisAFAP – attenuated FAPMAP – MYH associated polyposis

Question 29

What are the clinical features of HNPCC

Answer 29

Early but variable age at CRC diagnosis (~45 years)Tumor site throughout colon rather than descending colonExtracolonic cancers: endometrium, ovary, stomach, urinary tract, small bowel, bile ducts, sebaceous skin tumors

Question 30

What are clinical features of FAP?

Answer 30

Estimated penetrance for adenomas >90%Risk of extracolonic tumors (upper GI, desmoid, osteoma, thyroid, brain, other)CHRPE may be present Untreated polyposis leads to 100% risk of cancer

Question 31

Describe the effect of attenuated FAP

Answer 31

Later onset (CRC ~age 50)Few colonic adenomasNot associated with CHRPEUpper GI lesions Associated with mutations at 5’ and 3’ ends of APC gene

Question 32

What condition is similar to attenuated FAP?

Answer 32

Recessive MYH polyposisCommon mutations in mut- MYH gene

Question 33

What can Multiple modifier genes explain?

Answer 33

May explain families with history of cancer and no identified mutationMay explain differences in cancer penetrance in families with same mutation

Question 34

How can you manage caner risk in Adenomatous Polyposis syndromes?

Answer 34

SurveillanceSurgeryChemoprevention

Question 35

What portion of cancers are due to inherited mutations?

Answer 35

Only a small portion