Targeted therapy slows endometrial cancer growth in mice models

There may be a way to slow the growth of endometrial cancer through targeted cancer cell therapy, according to new research from the University of Missouri School of Medicine.

This year, around 65,000 women are expected to be diagnosed with endometrial cancer, the most common cancer of the female reproductive organs. An increased risk in development for multiple human cancers is associated with mutations in the PTEN protein, which normally regulates cell division and growth. The mutation allows cells to multiply uncontrollably. 

Using mice models, Krystina Dunston, research lab manager and NextGen Precision Health researchers Tae Hoon Kim and Jae-Wook Jeong, studied the use of targeted cancer cell therapy in mice with a PTEN mutation. They found that by targeting and silencing a specific gene expression, ERBB2, the chances of stopping tumor growth significantly increased. ERBB2 is one of the many genes that regulate cell growth. 

ERBB2 and PTEN are a part of different signaling pathways, but we believe they have a correlation in endometrial cancer. The effect of ERBB2 targeting on endometrial cancer with PTEN mutation is essential to understanding the mechanisms of how tumors grow in this type of cancer." 

Krystina Dunston, research lab manager 

Signaling pathways help amplify initial signals to cells, which trigger cell responses. This then acts similarly to the downstream effect, where the cell response causes another activation, and so on. 

Slowing the growth of endometrial cancer keeps multiple treatment options available. Currently, the standard treatment is a hysterectomy. More advanced stages would require aggressive treatments like radiation therapy and chemotherapy.

"All of these treatments can affect fertility, which is why it is important to find alternative ways to treat and prevent this disease," Dunston said. 

Krystina Dunston is a research laboratory manager at the NextGen Precision Health Center for Tae Hoon Kim and Jae-Wook Jeong's laboratories. Kim is an assistant professor of obstetrics, gynecology and women's health and earned his PhD at Chung-An University. Jeong is a Dr. R. Philip and Diane Acuff Endowed Professor of obstetrics, gynecology and women's health and received his PhD from Korea University. 

"ERBB2 Targeting Reveals a Significant Suppression of Tumorigenesis in Murine Endometrial Cancer with Pten Mutation" was recently published in Reproductive Sciences, a journal published by the Society for Reproductive Investigation. In addition to Dunston, Kim and Jeong, study authors from MU Health Care included Dr. Mark Hunter, a gynecologic oncologist and Dr. Eric Johannesen, a pathologist. Co-authors Jin-Seok Jung and Jung-Yoon Yoo also contributed. 

Source:
Journal reference:

Dunston, K., et al. (2024). ERBB2 Targeting Reveals a Significant Suppression of Tumorigenesis in Murine Endometrial Cancer with Pten Mutation. Reproductive Sciences. doi.org/10.1007/s43032-024-01546-3.

Comments

The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
Post a new comment
Post

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.

You might also like...
Early Phase I data shows promise for mRNA cancer immunotherapy in advanced solid cancers