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MACC1-从基因发现到临床转化的关键转移分子的第一个十年。

MACC1-the first decade of a key metastasis molecule from gene discovery to clinical translation.

机构信息

Experimental and Clinical Research Center, Charité-Universitätsmedizin Berlin and Max-Delbrück-Center for Molecular Medicine, Robert-Rössle-Straße 10, 13125, Berlin, Germany.

German Cancer Consortium (DKTK), German Cancer Research Center, Heidelberg, Germany.

出版信息

Cancer Metastasis Rev. 2018 Dec;37(4):805-820. doi: 10.1007/s10555-018-9771-8.

Abstract

Deciphering the paths to metastasis and identifying key molecules driving this process is one important issue for understanding and treatment of cancer. Such a key driver molecule is Metastasis Associated in Colon Cancer 1 (MACC1). A decade long research on this evolutionarily conserved molecule with features of a transcription factor as well as an adapter protein for versatile protein-protein interactions has shown that it has manifold properties driving tumors to their metastatic stage. MACC1 transcriptionally regulates genes involved in epithelial-mesenchymal transition (EMT), including those which are able to directly induce metastasis like c-MET, impacts tumor cell migration and invasion, and induces metastasis in solid cancers. MACC1 has proven as a valuable biomarker for prognosis of metastasis formation linked to patient survival and gives promise to also act as a predictive marker for individualized therapies in a broad variety of cancers. This review discusses the many features of MACC1 in the context of the hallmarks of cancer and the potential of this molecule as biomarker and novel therapeutic target for restriction and prevention of metastasis.

摘要

解析转移的途径并确定驱动该过程的关键分子是理解和治疗癌症的一个重要问题。这种关键驱动分子是结肠癌转移相关基因 1(MACC1)。对这种具有转录因子特征以及多功能蛋白-蛋白相互作用适配器蛋白的进化上保守分子进行了长达十年的研究,表明它具有多种特性,可以促使肿瘤进入转移阶段。MACC1 转录调控涉及上皮-间充质转化(EMT)的基因,包括那些能够直接诱导转移的基因,如 c-MET,影响肿瘤细胞的迁移和侵袭,并在实体瘤中诱导转移。MACC1 已被证明是与患者生存相关的转移形成预后的有价值的生物标志物,并有望作为广泛多种癌症个体化治疗的预测标志物。本文讨论了 MACC1 在癌症特征以及该分子作为生物标志物和新型治疗靶点以限制和预防转移的许多特性。

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