1. You Are At:
  2. Home
  3. World News
  4. Scientists discover rare form of hereditary colon cancer

Scientists discover rare form of hereditary colon cancer

In a fresh revelation on one of the world’s most dreaded diseases, scientists have found that mutation in a gene can lead to a form of hereditary colon cancer. According to the researchers at University

India TV News Desk, London [ Published on: July 29, 2016 16:12 IST ]
Representative Image
Representative Image

In a fresh revelation on one of the world’s most dreaded diseases, scientists have found that mutation in a gene can lead to a form of hereditary colon cancer.

According to the researchers at University Hospital Bonn, a large number of genetic changes have been discovered in MSH3 gene in patients.

"The knowledge about molecular mechanisms which lead to cancer is also a precondition for the development of new targeted drugs," said Stefan Aretz from University of Bonn Hospital in Germany.

The formation of large numbers of polyps in the colon has a high probability of developing into colon cancer, if left untreated.

Colon polyps form like mushroom-shaped growths from the mucosa and are several millimeters to several centimetres in size.

They are benign and generally do not cause any symptoms - however, they can turn into malignant tumours (colon cancer).

Physicians refer to the development of a large number of polyps in the colon as "polyposis." Scientists have already discovered several genes associated with a polyposis.

"However, about one-third of families affected by the disease do not have any abnormalities in these genes," Aretz said.

Therefore, there would have to be even more genes involved in the formation of polyps in the colon.

Together with pathologists from the University Hospital Bonn, scientists from the Yale University School of Medicine in New Haven (USA), and the Frankfurt University Hospital.

The team working with Aretz investigated the genetic material (DNA) of more than 100 polyposis patients using blood samples.

In each patient, all of the about 20,000 protein-coding genes known were simultaneously examined.

In this process, the scientists filtered the rare, possibly relevant genetic changes out of the gigantic quantity of data, like the proverbial needle in a haystack.

In two patients, genetic changes (mutations) were discovered in the MSH3 gene on chromosome five, showed the findings published in the American Journal of Human Genetics.

The researchers believe that by investigating the MSH3 gene, a clear diagnosis can be made prospectively in some other, previously unexplained polyposis cases. Afterwards, healthy persons at risk in the family can be tested for the mutations.

(With Agency inputs)

Write a comment