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Regulation of cell proliferation and survival: convergence of protein kinases and caspases.

机译:细胞增殖和存活的调节:蛋白激酶和胱天蛋白酶的融合。

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摘要

Intricate networks of protein kinases are intimately involved in the regulation of cellular events related to cell proliferation and survival. In addition to protein kinases, cells also contain networks of proteases including aspartic-acid directed caspases organized in cascades that play a major role in the regulation of cell survival through their involvement in the initiation and execution phases of apoptosis. Perturbations in regulatory protein kinase and caspase networks induce alterations in cell survival and frequently accompany transformation and tumorigenesis. Furthermore, recent studies have documented that caspases or their substrates are subject to phosphorylation in cells illustrating a potential convergence of protein kinase and caspase signaling pathways. Interestingly, a number of caspase substrates are protected from cleavage when they are phosphorylated at sites that are adjacent to caspase cleavage sites. While it is theoretically possible that many distinct protein kinases could protect proteins from caspase-mediated cleavage, protein kinase CK2 is of particular interest because acidic amino acids, including aspartic acid residues that are recognized by caspases, are its dominant specificity determinants.
机译:复杂的蛋白激酶网络与细胞增殖和存活相关的细胞事件的调节密切相关。除蛋白激酶外,细胞还含有蛋白酶网络,其中包括天冬氨酸定向的胱天蛋白酶,这些酶呈级联形式,通过参与细胞凋亡的起始和执行阶段,在调节细胞存活中起主要作用。调节蛋白激酶和半胱天冬酶网络的扰动诱导细胞存活率的改变,并经常伴随转化和肿瘤发生。此外,最近的研究已经证明,胱天蛋白酶或其底物在细胞中经受磷酸化,说明了蛋白激酶和胱天蛋白酶信号传导途径的潜在收敛。有趣的是,当许多半胱天冬酶底物在与半胱天冬酶切割位点相邻的位点被磷酸化时,被保护免受切割。从理论上讲,许多独特的蛋白激酶可以保护蛋白免受caspase介导的裂解,但蛋白激酶CK2尤其令人关注,因为酸性氨基酸(包括被caspases识别的天冬氨酸残基)是其主要的特异性决定因素。

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