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Hope For New Therapies For Liver Cancer Following Development Of Mouse Model

Researchers have created the first mouse model demonstrating the role of a cancer promoting gene, Astrocyte elevated gene-1 (AEG-1), in hepatocellular carcinoma, or . The mouse model represents a critical step in understanding the molecular mechanisms of progression and could lead to novel therapies for the disease.

Insights from the mouse model were recently published in the journal Hepatology by a team of researchers led by Devanand Sarkar, M.B.B.S., Ph.D., at Virginia Commonwealth University (VCU) Massey Cancer Center, Blick Scholar and assistant professor in the Department of Human and Molecular Genetics and member of the (VIMM) at VCU School of Medicine. AEG-1 was originally cloned in the lab of the study’s co-author, , M.Ph., Ph.D., Thelma Newmeyer Corman Endowed Chair in Oncology Research and program co-leader of at Massey, professor and chair of the Department of Human and Molecular Genetics and director of VIMM.

“My colleagues and I have been researching the role of AEG-1 in cancer development for several years and have shown it is linked to a diverse array of cancers, including liver cancer,” says Sarkar. “This mouse model represents a breakthrough in our ability to test and translate our laboratory findings.”

The mouse model gave the researchers a deeper understanding of the role of AEG-1 in liver cancer. Sarkar and his team confirmed AEG-1 overexpression significantly accelerated the progression of liver cancer. It also caused steatosis, or fatty liver, a mechanism that promotes inflammation and . In addition, the mouse model substantiated laboratory findings that suggested that AEG-1 plays a role in protecting liver cancer cells from chemotherapeutic drugs and alters tumor angiogenesis, or the way that new blood vessels are formed within the tumor.

The researchers plan to use the model to further explore the molecular mechanisms by which AEG-1 promotes liver cancer, including the role of AEG-1 in fat metabolism and obesity-related diseases.

“This model moves us forward in the research process by allowing us to test a variety of compounds that could inhibit AEG-1 and prevent the development and progression of liver cancer,” says Sarkar. “Ultimately, we hope our efforts will lead to new therapies and save lives.”

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In addition to Fisher, Sarkar collaborated on this study with Jolene Windle, Ph.D., Catherine Dumur, Ph.D., Luni Emdad, Ph.D., Nitai Mukhopadhyay, Ph.D., and Philip Hylemon, Ph.D., from VCU Massey Cancer Center; Jyoti Srivastava, Ph.D., Ayesha Siddiq, Ph.D., Prasanna Kumar Santhekadur, Ph.D., Rachel Gredler, Ph.D. candidate, Xue-Ning Shen, M.D., Mark Subler, Ph.D., Chadia Robertson, Ph.D. candidate, and Jillian Stafflinger, lab specialist, from the Department of Human and Molecular Genetics at VCU School of Medicine; Dong Chen, M.D., from the Department of Pathology at VCU School of Medicine; Deepak Bhere, Ph.D., and Khalid Shah, Ph.D., from the Departments of Radiology and Neurology at Harvard Medical School; Rushdy Ahmad, Ph.D., from the Broad Institute of Harvard and Massachusetts Institute of Technology; and Shah Giashuddin, M.D., from New York Hospital Medical Center.
Funding for this study was provided by grant R01 CA138540 from the National Cancer Institute, grant R01 CA134721from the National Institutes of Health and grants from the James S. McDonnell Foundation and Samuel Waxman Cancer Research Foundation. The study was also supported, in part, with funding from VCU Massey Cancer Center’s NIH-NCI Cancer Center Support Grant P30 CA016059.
Virginia Commonwealth University