We've updated our Privacy Policy to make it clearer how we use your personal data. We use cookies to provide you with a better experience. You can read our Cookie Policy here.

Advertisement

Hepatitis B May Amplify Cancer Risk From Carcinogens

Interleukin 33 (brown) upregulation in hepatitis B virus-positive chronic hepatitis.
Credit: Shawn Demehri, Mass General Brigham
Listen with
Speechify
0:00
Register for free to listen to this article
Thank you. Listen to this article using the player above.

Want to listen to this article for FREE?

Complete the form below to unlock access to ALL audio articles.

Read time: 1 minute

Hepatitis B virus (HBV) infection is known to be associated with the risk of hepatocellular carcinoma (HCC), but how and why they are connected remains unknown. Researchers from Mass General Brigham discovered that HBV does not cause liver inflammation or cancer on its own, but worsens liver inflammation and may make patients more susceptible to early cancer development caused by environmental carcinogens. Limiting carcinogen exposure or reducing inflammation could mitigate this risk. The results are published in Nature Communications.


“Our research sheds light on the intricate interplay between HBV infection and carcinogen exposure to generate immune dysregulation in the liver that leads to cancer development,” said corresponding author Shawn Demehri, MD, PhD, of the Demehri Lab and Krantz Family Center for Cancer Research at Massachusetts General Hospital, a founding member of the Mass General Brigham healthcare system. “We propose the potential of combining statin therapy with conventional HBV treatments like entecavir to improve patient outcomes.”


Using a mouse model, the researchers found that HBV did not directly cause liver inflammation or cancer. However, when the HBV models were exposed to a carcinogen found in tobacco smoke, fried foods, processed meats, and alcoholic drinks, they developed an extreme liver cancer phenotype. This carcinogen, also known as diethylnitrosamine (DEN), caused an increase in interleukin-33 (IL-33), an inflammatory molecule, which is required for the development of liver cancer. The researchers then treated the models with pitavastatin, a statin drug, to suppress the expression of IL-33. This treatment was effective in reducing the risk of chronic hepatitis and liver cancer.


The researchers then extended their findings into humans, finding higher levels of IL-33, especially in patients with HBV-associated hepatitis, compared to healthy controls. They then looked at data from more than 200 million patients, finding that the risk of hepatitis and liver cancer were significantly reduced in patients treated with a statin compared with those treated with another cholesterol-lowering drug.


Reference: Huang M, Wang D, Huang J, et al. Hepatitis B virus promotes liver cancer by modulating the immune response to environmental carcinogens. Nat Commun. 2025;16(1):5360. doi: 10.1038/s41467-025-60894-z


This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source. Our press release publishing policy can be accessed here.