Genomic Study of Cervical Cancer Promises Disease Cure

A team of researchers has completed a comprehensive genomic analysis of cervical cancer in two patient populations.

And this has identified recurrent genetic mutations not previously found in the disease, including at least one for which targeted treatments have been approved for other forms of cancer.

Cervical Cancer - Types, Causes, Symptoms, Diagnosis, Treatment, Complications & Prevention
Cancer cervix refers to cancerous growth in the cervix and usually occurs in the transition called squamo-columnar junction.

The study by researchers from the Boston area, Mexico, and Norway also shed light on the role human papillomavirus (HPV) plays in the development of cervical cancer.

To investigate the genomic underpinnings of the disease, the team performed whole exome sequencing, which examines the genetic code in the protein-coding regions of the genome, on samples from 115 cervical cancer patients from Norway and Mexico.

In some cases, the researchers also conducted whole genome sequencing (analyzing the genetic code across the entire genome) or transcriptome sequencing (focusing on gene expression).

Pap smear and Cervical Cancer Screening
Pap smear is the most common test used in screening cervical cancer caused by an infection with human papilloma virus. Pap smear should be repeated every 1 to 3 years till the age of 65 years.

In each case, the researchers compared genomic data derived from cervical cancer tumours with genomic data from healthy tissue from the same individual to determine what may have gone wrong - or mutated - in the genome to allow the cancer to develop. The mutations identified in tumours but not in healthy tissues from the same individuals are referred to as somatic mutations.

The study identified 13 mutations that occurred frequently enough across the samples to be considered significant in cervical cancer. Eight of these mutations had not been linked to the disease previously, and two had not previously been seen in any cancer type.

Expert Says Timely Tests can Cut Cervical Cancer by a Third
Health expert says that diagnostic tests for human papilloma virus (HPV) can cut by a third the incidence of cervical cancer in women worldwide.

Among the most notable findings were somatic point mutations in the gene ERBB2, which was found in a small but significant subset of the tumours. Mutations in this gene, which is also known as Her-2, had not been previously been linked to cervical cancer, but it is a known oncogene common in breast cancer. Treatments exist that target the gene.

The team also identified a novel mutation in the gene MAPK1. MAPK1 is one of the final steps in the MAP kinase signaling pathway - a network of interconnected genes that play a role in cell growth regulation.

Cervical Cancer Screenings Overused in Almost Two-Thirds of Women
Clinicians throughout the United States have been performing unnecessary Pap tests for cervical cancer screening in certain groups of women for the past ten years.

Another key finding was the prevalence of mutations in genes affecting the immune system.

Finally, transcriptome sequencing, which allowed the team to analyze gene expression - how and when genes are activated across the genome - enabled the researchers to learn more about how HPV is driving cervical cancer.

The study is published in journal Nature.

Source-ANI