City
Epaper

Interrupting RNA activity can improve survival chances in pancreatic cancer patients

By ANI | Updated: April 24, 2021 17:25 IST

During a recent study, researchers uncovered a molecular pathway that enhances chemotherapy resistance in some pancreatic cancer patients. A patient's response to therapy and their overall survival chance can be increased by targeting an RNA to interrupt its activity.

Open in App

During a recent study, researchers uncovered a molecular pathway that enhances chemotherapy resistance in some pancreatic cancer patients. A patient's response to therapy and their overall survival chance can be increased by targeting an RNA to interrupt its activity.

The study led by Nagoya University researchers and colleagues in Japan was published in the journal Cancer Research.

"Pancreatic cancer is one of the most aggressive human malignancies, with an overall med ian survival that is less than five months," says cancer biologist Yutaka Kondo of Nagoya University Graduate School of Medicine. "This poor prognosis is partially due to a lack of potent therapeutic strategies against pancreatic cancer, so more effective treatments are urgently needed."

Kondo and his colleagues focused their attention on a long noncoding RNA (lncRNA) called taurine upregulating gene 1 (TUG1). lncRNAs are gene regulators, several of which have recently been identified for helping some cancers resist chemotherapy. TUG1 is already known for being overexpressed in gastrointestinal cancers that have a poor prognosis and are resistant to chemotherapy.

The researchers found TUG1 was overexpressed in a group of patients with pancreatic ductal adenocarcinoma. These patients were resistant to the standard chemotherapy treatment 5-fluorouracil (5-FU), and died much sooner compared to cancer patients with low TUG1 expression levels.

Further laboratory tests showed TUG1 counteracts a specific microRNA, leading to increased activity of an enzyme, called dihydropyrimidine dehydrogenase, which breaks down 5-FU into a compound that can't kill cancer cells.

Kondo and his team found they could suppress TUG1 during 5-FU treatment of mice with pancreatic cancer by using antisense oligonucleotides attached to a specially designed cancer-targeting drug delivery system. Antisense oligonucleotides interfere with gene expression.

"Our data provides evidence that our therapeutic approach against pancreatic cancer could be promising," says Kondo.

The team now plans to conduct further laboratory investigations to test the effectiveness of their therapeutic strategy.

( With inputs from ANI )

Disclaimer: This post has been auto-published from an agency feed without any modifications to the text and has not been reviewed by an editor

Tags: Cancer ResearchNagoya universityYutaka kondo
Open in App

Related Stories

InternationalJapanese researchers find new way to diagnose ovarian cancer

TechnologyStudy gives new insight into diagnosing ovarian cancer

HealthUnidentified proteins indicate a potential method for ovarian cancer diagnosis: Study

TechnologyDiet of nematodes affects capacity to learn: Study

HealthEndometriosis may be caused by bacterial infections: Study

Technology Realted Stories

TechnologyZoho CEO Sridhar Vembu has no ‘confidence in tech’, shelves $700 million chip plan

TechnologyYouTube commits Rs 850 crore to power India’s ‘Creator Nation’: CEO Neal Mohan

TechnologyApple clocks 28 pc growth in iPhone shipments in India: Industry data

TechnologyNHRC asks 11 states to boost measures to prevent heat-related deaths

TechnologyNRAI and ONDC refute speculative reports, reaffirm strong partnership