Shinji Matsumoto, Akira Kikuchi ≪Molecular Biology and Biochemistry≫ Breast cancer gene a potential target for childhood liver cancer treatment
2019-08-27 Publish Nature Communications Researchers from Osaka University find that a gene normally involved in hormone-induced growth of breast cancer cells is also a key player in the development of hepatoblastoma Hepatoblastoma is a rare form of liver cancer affecting just a few individuals per million. However, it is the leading cause of liver cancer in infants and young children, with most patients diagnosed before their third birthday. While advances in surgery and chemotherapy have meant that the prognosis for hepatoblastoma patients is generally quite good, aggressive forms of the disease leave some young patients with few treatment options and poor long-term survival rates. In a study published at 18:00 (JST) on Aug. 28 in Nature Communications, researchers from Osaka University have built on prior research to make a breakthrough in our understanding of the causes of hepatoblastoma, identifying a gene that could be key to developing a targeted therapy. As far back as 1999, researchers realized that a large number of hepatoblastoma patients—up to 90% in some cases—carry mutations in a gene called β-catenin. As part of the Wnt/β-catenin signaling pathway, the β-catenin protein activates genes needed for cellular growth and differentiation. If left unchecked, β-catenin accumulation can result in tumor formation. Mutations in Wnt/β-catenin signaling components often lead to β-catenin accumulation and are common in several forms of cancer. “We decided to screen uncharacterized Wnt/β-catenin target genes in liver tumor cells to try and identify novel genes with a role in the development of hepatoblastoma,” explains lead author of the study Shinji Matsumoto. “One of the most abundantly expressed genes was growth regulation by estrogen in breast cancer 1 (GREB1), which is a well-known estrogen-responsive gene implicated in the growth of breast cancer cells.” While well-characterized in breast cancer, no one had determined that GREB1 was actually a target of Wnt/β-catenin signaling, and its role in non-hormone-sensitive tumor development was unconfirmed. But after studying the protein in more detail, it became obvious to the researchers that GREB1 could be a major player in the development of hepatoblastoma. “Overexpression of β-catenin in a mouse liver cancer model resulted in tumor formation and an increase in GREB1 expression,” says corresponding author Akira Kikuchi. “If we then suppressed the production of GREB1, we saw a decrease in hepatoblastoma cell proliferation and therefore fewer tumors in the study animals.” Because GREB1 is active in the nucleus, the researchers attempted to prevent tumor formation using amido-bridged nucleic acid-modified antisense oligonucleotides. These small single-stranded DNA molecules specifically interfere with the production of target proteins by binding to the mRNA. Significantly, the GREB1-targeted oligonucleotides successfully decreased GREB1 production and suppressed the formation of hepatoblastoma tumors. Using this strategy, it is hoped that a GREB1-targeted therapy can now be developed to specifically treat hepatoblastoma. ### The article, “GREB1 induced by Wnt signaling promotes development of hepatoblastoma by suppressing TGFβ signaling,” was published in Nature Communications at DOI: https://doi.org/10.1038/s41467-019-11533-x Summary: Hepatoblastoma is a rare liver cancer that mainly affects infants and young children and is associated with mutations in the β-catenin gene. Researchers from Osaka University screened uncharacterized targets of Wnt/β-catenin signaling and confirmed that breast cancer gene GREB1 plays a major role in hepatoblastoma cell proliferation. By interfering with GREB1 protein production, tumor formation was inhibited in a mouse liver cancer model, suggesting this approach could be used to develop a targeted hepatoblastoma therapy. Primary Keyword: Medicine/Health Authors: Shinji Matsumoto, Taku Yamamichi, Koei Shinzawa, Yuuya Kasahara, Satoshi Nojima, Takahiro Kodama, Satoshi Obika, Tetsuo Takehara, Eiichi Morii, Hiroomi Okuyama, and Akira Kikuchi DOI: 10.1038/s41467-019-11533-x About Osaka University Osaka University was founded in 1931 as one of the seven imperial universities of Japan and now has expanded to one of Japan’s leading comprehensive universities. The University has now embarked on open research revolution from a position as Japan’s most innovative university and among the most innovative institutions in the world according to Reuters 2015 Top 100 Innovative Universities and the Nature Index Innovation 2017. The university’s ability to innovate from the stage of fundamental research through the creation of useful technology with economic impact stems from its broad disciplinary spectrum. Website: https://resou.osaka-u.ac.jp/en/top
Additional Keywords: Cancer, Liver, Pediatrics, Molecular Biology, Genetics
Title: GREB1 induced by Wnt signaling promotes development of hepatoblastoma by suppressing TGFβ signaling
Journal: Nature Communications
Funded by: Ministry of Education, Culture, Sports, Science and Technology
