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The Role of the Metzincin Superfamily in Prostate Cancer Progression: A Systematic-Like Review

机译:甲氧锌素超家族在前列腺癌进展中的作用:系统化的评论

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摘要

Prostate cancer remains a leading cause of cancer-related morbidity in men. Potentially important regulators of prostate cancer progression are members of the metzincin superfamily of proteases, principally through their regulation of the extracellular matrix. It is therefore timely to review the role of the metzincin superfamily in prostate cancer and its progression to better understand their involvement in this disease. A systematic-like search strategy was conducted. Articles that investigated the roles of members of the metzincin superfamily and their key regulators in prostate cancer were included. The extracted articles were synthesized and data presented in tabular and narrative forms. Two hundred and five studies met the inclusion criteria. Of these, 138 investigated the role of the Matrix Metalloproteinase (MMP) subgroup, 34 the Membrane-Tethered Matrix Metalloproteinase (MT-MMP) subgroup, 22 the A Disintegrin and Metalloproteinase (ADAM) subgroup, 8 the A Disintegrin and Metalloproteinase with Thrombospondin Motifs (ADAMTS) subgroup and 53 the Tissue Inhibitor of Metalloproteinases (TIMP) family of regulators, noting that several studies investigated multiple family members. There was clear evidence that specific members of the metzincin superfamily are involved in prostate cancer progression, which can be either in a positive or negative manner. However, further understanding of their mechanisms of action and how they may be used as prognostic indicators or molecular targets is required.
机译:前列腺癌仍然是男性癌症相关的发病率的主要原因。前列腺癌进展的潜在重要调节剂是蛋白酶甲磺夹蛋白的成员,主要是通过它们对细胞外基质的调节。因此,它及时审查甲氧化嘧啶超家族在前列腺癌中的作用及其进展,以更好地了解他们对这种疾病的参与。进行了系统的搜索策略。调查甲氧化嘧啶超家族成员和其关键调节剂在前列腺癌中的作用的文章。综合提取的制品,并以表格和叙事形式呈现的数据。二百五项研究达到了纳入标准。其中,138研究了基质金属蛋白酶(MMP)亚组的作用,34个膜系重基质金属蛋白酶(MT-MMP)亚组,22例脱胶苷和金属蛋白酶(ADAM)亚组,8个具有血小板素基序的解体素和金属蛋白酶(Adamts)亚组和53组织抑制剂(TIMP)调节因子的组织抑制剂,注意到几项研究调查了多个家庭成员。有明确的证据表明,甲氧锌素超家族的特定成员参与前列腺癌进展,这可以是正面或负面的方式。但是,需要进一步了解它们的作用机制以及如何用作预后指标或分子靶标。

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