Gene 210 Cancer Genomics May 5, 2015

Key events in investigating the cancer genome M R Stratton Science 2011;331:

Flow chart of the genome analysis for a cancer patient O Kilpivaara, and L A Aaltonen Science 2013;339:

Today’s Plan Genetics of common cancers (rare variants and common variants) Colorectal cancer Prostate cancer Lung cancer Melanoma Breast cancer BRCA1 and BRCA2 genes Robin Starr **Break** Linking somatic genetic alterations in cancer to targeted therapeutics Class exercise

Colorectal Cancer 3 rd most common form of cancer in developed world (excluding skin cancers) Life time risk of developing colorectal cancer is ~5%

Colorectal Cancer Most colorectal cancers usually begin as a non-cancerous polyp on the inner lining of the colon or rectum ~95% of colorectal cancers are adenocarcinomas

Inherited colorectal cancer syndromes 5-10% of colorectal cancers are caused by inherited gene mutations Familial adenomatous polyposis (FAP) Caused by mutations in the APC gene ~1% of all colorectal cancer cases due to FAP Hereditary non-polyposis colon cancer (HNPCC; Lynch syndrome) Caused by mutations in DNA damage repair genes HNPCC, also known as Lynch syndrome, accounts for about 3-5% of all colorectal cancers

Individuals with FAP usually develop hundreds or thousands of polyps in their colon and rectum Cancer usually develops in 1 or more polyps as early as age 20 By age 40, most people with this disorder will develop cancer Surgery to remove colon is a preventive treatment for FAP individuals Familial adenomatous polyposis (FAP)

Inherited colorectal cancer syndromes 5-10% of colorectal cancers are caused by inherited gene mutations Familial adenomatous polyposis (FAP) Caused by mutations in the APC gene ~1% of all colorectal cancer cases due to FAP Hereditary non-polyposis colon cancer (HNPCC; Lynch syndrome) Caused by mutations in DNA damage repair genes HNPCC, also known as Lynch syndrome, accounts for about 3-5% of all colorectal cancers due to Lynch syndrome

Not as many polyps as FAP individuals ~80% lifetime risk of developing colorectal cancer Mutations in MLH1, MSH2, MSH6, and PMS2, which encode proteins involved in DNA repair Hereditary non-polyposis colon cancer Expression of hMSH2 causes a dominant mutator phenotype in E. coli (Fisher et al., Cell 1993)

14 common variants associated with increased risk of colorectal cancer Houlston et al., Nat Genet 2010 Lubbe et al., Hum Mol Genet 2011

Prostate Cancer Most common cancer in men 1 in 6 lifetime risk Large genetic component (42%)

Multiple prostate cancer risk variants on 8q24 Witte Nat Genet 2007

12 common variants associated with increased risk of prostate cancer Estes et al., Nat Genet 2009 Takata et al., Nat Genet 2010

Lung Cancer #1 cause of cancer deaths in United States ~90% of lung cancer caused by smoking Heritability of lung cancer 8-14%

A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25 Thorgeirsson et al., Nature 2008 Amos et al., Nat Genet 2008 Hung et al., Nature 2008

Melanoma (Skin Cancer) Only accounts for <5% of skin cancers but responsible for most skin cancer deaths Heritability of lung cancer 18-21%

Common variants that confer risk for melanoma Hayward Oncogene 2003 Melanocortin-1 receptor: G-protein- coupled receptor expressed in melanocytes. Variants in MC1R associated with red hair and fair skin

Breast Cancer 2 nd most common cancer in women (next to skin cancer) 2 nd leading cause of cancer deaths in women Heritability of lung cancer 27-40%

Science, 1990 Science, 1994

BRCA1 and BRCA2 5-10% of breast cancer is inherited (mostly due to BRCA1/2 mutations) Also increases risk of ovarian cancer 23andMe reports 3 known BRCA mutations common in Ashkenzai Jewish population 185delAG (BRCA1) – increases lifetime risk of breast cancer from 12% to 60% and ovarian cancer from 2% to 40% 5382insC (BRCA1) – increases lifetime risk of breast cancer from 12% to 60% and ovarian cancer from 2% to 40% 6174delT (BRCA2) – increases lifetime risk of breast cancer from 12% to 50% and ovarian cancer from 2% to 20% By age 70, 50-60% of women who have a BRCA mutation will develop breast cancer and 20-40% will develop ovarian cancer BRCA1 and BRCA2 encode proteins that repair DNA double-strand breaks

Patenting Genes?

Discussion with Robin Starr

BREAK

Somatic mutations in cancer

Key events in investigating the cancer genome M R Stratton Science 2011;331:

B Vogelstein et al. Science 2013;339: Number of somatic mutations in various cancers

Flow chart of the genome analysis for a cancer patient O Kilpivaara, and L A Aaltonen Science 2013;339:

The Cancer Genome Benefits and applications of cancer genome sequencing? 1.Tumor heterogeneity 2.Design treatments based on tumor sequence 3.Response to therapy

Linking somatic genetic alterations in cancer to targeted therapeutics

Chronic myelogenous leukemia Philadelphia chromosome formed by a translocation t(9;22) Generates the BCR-ABL oncogene Constitutively active c-ABL kinase activity Imatinib (Gleevec) Dramatic therapeutic benefit 6-year survival rates ~90%

BRAF mutations in melanoma Nature % of malignant melanomas 80% have same mutation (V600E), which increases kinase activity

BRAF inhibitors

Key events in investigating the cancer genome M R Stratton Science 2011;331:

DNA copy number arrays DNA methylation Exome sequencing Transcriptome microRNA profiling Proteomics

Class Exercise You work for a new genome interpretation startup company Your first customer sends you tumor biopsy DNA samples from 8 cancer patients You perform genomic analyses on tumor biopsies and generate exome sequence and expression analyses for several major cancer susceptibility genes for each patient (cytogenetic analysis; DNA sequence for BRCA1, BRCA2, EGFR, BRAF; expression analysis for estrogen receptor, HER2, MET) Use personalized tumor genetic profile to suggest appropriate targeted therapy Discuss rationale for each therapeutic choice (what is genetic lesion? What defect (e.g. signaling pathway) does this cause? What does the chosen therapy target?)