| Literature DB >> 33239430 |
Minhong Shen1, Shanshan Xie1,2,3,4, Michelle Rowicki1, Sven Michel5, Yong Wei1, Xiang Hang1, Liling Wan1, Xin Lu1, Min Yuan1, John F Jin6, Frank Jaschinski5, Tianhua Zhou4,7,8, Richard Klar5, Yibin Kang9,10.
Abstract
Colorectal and lung cancers account for one-third of all cancer-related deaths worldwide. Previous studies suggested that metadherin (MTDH) is involved in the development of colorectal and lung cancers. However, how MTDH regulates the pathogenesis of these cancers remains largely unknown. Using genetically modified mouse models of spontaneous colorectal and lung cancers, we found that MTDH promotes cancer progression by facilitating Wnt activation and by inducing cytotoxic T-cell exhaustion, respectively. Moreover, we developed locked nucleic acid-modified (LNA) MTDH antisense oligonucleotides (ASO) that effectively and specifically suppress MTDH expression in vitro and in vivo. Treatments with MTDH ASOs in mouse models significantly attenuated progression and metastasis of colorectal, lung, and breast cancers. Our study opens a new avenue for developing therapies against colorectal and lung cancers by targeting MTDH using LNA-modified ASO. SIGNIFICANCE: This study provides new insights into the mechanism of MTDH in promoting colorectal and lung cancers, as well as genetic and pharmacologic evidence supporting the development of MTDH-targeting therapeutics. ©2020 American Association for Cancer Research.Entities:
Mesh:
Substances:
Year: 2020 PMID: 33239430 PMCID: PMC8026491 DOI: 10.1158/0008-5472.CAN-20-1876
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 13.312