Genetic Mutations Linked to Rare Multiple Bowel Tumors

They analyzed 20 synchronous colorectal cancers (syCRC) from 10 patients, and compared their genetics to people with only one colorectal cancer and to healthy people.

Tumors used in this study were collected from patients diagnosed with CRC who underwent surgical resection of two syCRC in a window of time of six months maximum. Five mononucleotides were analyzed by capillary gel electrophoresis and used as molecular markers of microsatellite instability in tumors of four patients. A tumor was classified as microsatellite unstable when at least one marker was found altered. Genomic DNA for all tumors, except one patient and seven matched normal tissues was extracted from 10 μm-thick formalin-fixed paraffin embedded (FFPE) sections using QIAamp DNA FFPE Tissue kit (Qiagen, Hilden, Germany). DNA from blood and frozen samples was also extracted. Libraries were sequenced using either HiSeq 2000 or HiSeq 2500 (Illumina, San Diego, CA, USA).

The genetic analysis found the synchronous tumors were not related to each other as they contained a variety of different genetic mutations that had led to cancer. This genetic variation makes synchronous colorectal cancers more difficult to treat, because therapies targeted at specific genetic aberrations in a person's cancer may not work if the other tumor has different genetic mutations. The team also found synchronous colorectal cancer patients had a higher occurrence of inherited damaging mutations in immune-related genes. Three-quarters of synchronous colorectal cancer patients were found to have rare damaging mutations in genes related to immune system function.

These patients had differences in the composition of their gut immune cells, which could lead to inflammation in the gut. The study authors conclude that synchronous colorectal cancer patients have inherited damaging alterations of immune-related genes, which may cause an inflammatory environment in the gut and increase the frequency of independent cancer-initiating events. The study was published on July 5, 2016, in the journal Nature Communications.

Related Links:
King's College London
FIRC Institute of Molecular Oncology
Qiagen
Illumina