Newswise — WASHINGTON (January 20, 2020) — Mice given a new drug targeting a key gene involved in lipid and glucose metabolism could tolerate a high-fat diet regimen (composed of 60% fat from lard) without developing significant liver damage, becoming obese, or disrupting their body’s glucose balance. The study by Georgetown Lombardi Comprehensive Cancer Center researchers appeared January 20, 2020, in Cell Death and Differentiation.

The U.S. Centers for Disease Control and Prevention (CDC) estimates that there are 4.5 million adults in the U.S. diagnosed with liver disease every year. Nonalcoholic fatty liver disease, or NAFLD, can evolve to a more serious condition known as inflammatory steatohepatitis, or NASH, which can lead to chronic inflammation, scarring of the liver, and cirrhosis and eventually to hepatocellular carcinoma. While NAFLD can be reversed in the early stages with weight loss and dietetic adjustments, it becomes intractable in later stages.

There is no standard therapy for NASH, albeit many drugs are being evaluated in clinical trials.  Because of the now epidemic state of the liver disease, researchers at Georgetown developed a small molecule able to inhibit the activity of a key gene, Slc25a1, that they hypothesized plays an important role in fatty liver disease.

“Our research takes on a definite urgency when you consider that about 25 percent of adults in the U.S. have NAFLD,” said Maria Laura Avantaggiati, MD, associate professor of oncology at Georgetown Lombardi. In addition, while NAFLD can be reversed with dietetic adjustments, it is difficult for these individuals to undergo dramatic life-style changes, posing a challenge to halt NAFLD evolution to NASH.”

One of the investigators’ key steps was to administer the new drug, CTPI-2, as a preventive treatment in mice fed the high-fat diet before NASH developed, or as a reversion treatment in mice with significant liver damage. This latter setting reflects what is seen people who seek medical advice when the disease is already present. The administration of CTPI-2 was able to nearly completely prevent the evolution to NASH and obesity in mice on the high-fat diet, compared to mice that did not receive the drug. At later stages of the disease, CTPI-2 also reversed liver damage, induced weight loss and restored the glucose metabolic profile.

“The results were quite dramatic as the livers of most of the mice that received CTPI-2 nearly resembled the normal livers of animals fed with a regular diet,” said Avantaggiati. “In addition, CTPI-2 normalized glucose metabolism, leading us to hypothesize that the drug could also have applications in the treatment of diabetes, but this aspect will need further study.”

To confirm their findings, the investigator developed a genetically modified mouse with Slc25a1 inactivated in the liver. Mice with the inactive Slc25a1 gene were partially protected from fatty liver disease as if they were treated with CTPI-2, confirming the importance of this gene in liver damage induced by the high-fat diet.

“We have established that CTPI-2 has anti-inflammatory activity and has anti-tumor activity towards several types of cancer, said Avantaggiati. “We now need to establish if CTPI-2 can also halt the progression to hepatocellular carcinoma.”

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In addition to Avantaggiati, authors from Georgetown University include Mingjun Tan, Garrett T. Graham, Anna Kasprzyk-Pawelec, Shreyas Gadre, Erika Parasido, Olga Catalina-Rodriguez, Patricia Foley, Giuseppe Giaccone, Amrita Cheema, Bhaskar Kallakury, Chris Albanese and Chunling Yi and Rami Mosaoa, who also has an appointment at  King Abdulaziz University, Saudi Arabia.

Georgetown University has a patent application directed to this research with Avantaggiati named as an inventor.

This research was supported by NIH grants (RO1 CA1923698 and R21 DE028670).

Tan M, et al. Inhibition of the mitochondrial citrate carrier, Slc25a1, reverts steatosis, glucose intolerance and inflammation in preclinical models of NAFLD/NASH. Cell Death and Differentiation. 20 Jan. 2020.

About Georgetown Lombardi Comprehensive Cancer Center Georgetown Lombardi Comprehensive Cancer Center is designated by the National Cancer Institute (NCI) as a comprehensive cancer center. A part of Georgetown University Medical Center, Georgetown Lombardi is the only comprehensive cancer center in the Washington D.C. area. It serves as the research engine for MedStar Health, Georgetown University’s clinical partner. Georgetown Lombardi is also an NCI recognized consortium with John Theurer Cancer Center/Hackensack Meridian Health in Bergen County, New Jersey. The consortium reflects an integrated cancer research enterprise with scientists and physician-researchers from both locations. Georgetown Lombardi seeks to improve the diagnosis, treatment, and prevention of cancer through innovative basic, translational and clinical research, patient care, community education and outreach to service communities throughout the Washington region, while its consortium member John Theurer Cancer Center/Hackensack Meridian Health serves communities in northern New Jersey. Georgetown Lombardi is a member of the NCI Community Oncology Research Program (UG1CA239758). Georgetown Lombardi is supported in part by a National Cancer Institute Cancer Center Support Grant (P30CA051008). Connect with Georgetown Lombardi on Facebook (Facebook.com/GeorgetownLombardi) and Twitter (@LombardiCancer).

About Georgetown University Medical Center
Georgetown University Medical Center (GUMC) is an internationally recognized academic health and science center with a four-part mission of research, teaching, service and patient care (through MedStar Health). GUMC’s mission is carried out with a strong emphasis on public service and a dedication to the Catholic, Jesuit principle of cura personalis -- or “care of the whole person.” The Medical Center includes the School of Medicine and the School of Nursing & Health Studies, both nationally ranked; Georgetown Lombardi Comprehensive Cancer Center, designated as a comprehensive cancer center by the National Cancer Institute; and the Biomedical Graduate Research Organization, which accounts for the majority of externally funded research at GUMC including a Clinical and Translational Science Award from the National Institutes of Health.  Connect with GUMC on Facebook (Facebook.com/GUMCUpdate), Twitter (@gumedcenter).

 

 

 

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CITATIONS

RO1 CA1923698 and R21 DE028670; Cell Death and Differentiation