Colorectal cancer (CRC) is a formidable health problem worldwide and fourth most common cause of death due to cancer. In India, the annual incidence rates (AARs) for colon cancer and rectal cancer in men are 4.4 and 4.1 per 100000, respectively.
An estimated 10% -15% of these cancers are likely attributable to hereditary (germline) causes. Several genes are associated with an increased risk of developing CRC, and those of key interest include those for Lynch syndrome, MLH1, MSH2, MSH6, PMS2, EPCAM; adenomatous polyposis conditions (APC), MUTYH, POLE, POLD1; hamartomatous polyposis syndromes PTEN, SMAD4, STK11, and other rare cancer predisposition states where colorectal cancer is part of the phenotype, CHEK2 and TP53.
The National Comprehensive Cancer Network™ (NCCN) guidelines provide recommendations for investigating MSI by PCR and/or MMR by IHC for 15 different cancer types
Other environmental factors include: Age, gender (male), ulcerative colitis, alcohol, obesity etc.
APC BRAF CDKN2A ERBB2 KRAS MLH1 MSH2 MSH6 NRAS PIK3CA PMS2 POLE PTEN SMAD4 TP53 MUTYH STK11 EPCAM BMPR1A CHEK2 POLD1
We offer several cancer panels depending upon the needs of the Oncologists, these include..
BRCA panel for testing mutations in BRCA1 and BRCA2 genes
Lung RNA fusion panel for detecting gene fusions in major driver genes
Profiling of 15 genes associated with hereditary Breast and Ovarian cancer, pancreatic and prostate cancer
Profiling of >140 genes associated with inherited cancers