Peking University Health Science Center, Department of Anatomy, Histology and Embryology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), and State Key Laboratory of Natural and Biomimetic Drugs, Beijing 100191, China.
Peking University Health Science Center, Department of Anatomy, Histology and Embryology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), and State Key Laboratory of Natural and Biomimetic Drugs, Beijing 100191, China.
Int J Biochem Cell Biol. 2018 May;98:93-103. doi: 10.1016/j.biocel.2018.03.008. Epub 2018 Mar 12.
The Kindlins are FERM domain proteins comprising three members (Kindlin-1, -2 and -3) which are evolutionarily conserved. Kindlins bind with β-integrin cytoplasmic tails and execute broad biological functions including directed cell migration, proliferation, differentiation and survival. In light of more and more evidence point to the importance of Kindlin family members in normal development and human diseases especially in cancers, we aim to portrait the profile of Kindlins in the regulation of embryonic development and cancer progression. We first summarize all the known binding proteins for individual member of Kindlin family. We then outline the Kindlin-regulated signaling pathways including Wnt/β-catenin, TGFβ, EGFR, and Hedgehog signalings. Furthermore, we descript the pivotal role of Kindlins in embryonic development in detail with notions that Kindlin-1 is highly expressed in endo/ectodermal originated tissues, Kindlin-2 is highly expressed in mesoderm-derived tissues and Kindlin-3 is highly expressed in mesoderm- and ectoderm-derived tissues. Deregulation of Kindlins is generally reported in cancers from different organs. We also briefly descript the role of Kindlins in other diseases. Finally, we update the recent understanding of how Kindlins are regulated and modified as well as the degradation mechanism of Kindlins, respectively.
Kindlins 是 FERM 结构域蛋白,包含三个成员(Kindlin-1、-2 和 -3),它们在进化上是保守的。Kindlins 与 β-整联蛋白胞质尾部结合,并执行广泛的生物学功能,包括定向细胞迁移、增殖、分化和存活。鉴于越来越多的证据表明 Kindlin 家族成员在正常发育和人类疾病中特别是在癌症中具有重要作用,我们旨在描绘 Kindlins 在胚胎发育和癌症进展中的调控作用。我们首先总结了 Kindlin 家族每个成员的所有已知结合蛋白。然后概述了 Kindlin 调节的信号通路,包括 Wnt/β-catenin、TGFβ、EGFR 和 Hedgehog 信号通路。此外,我们详细描述了 Kindlins 在胚胎发育中的关键作用,并提出以下观点:Kindlin-1 在内外胚层起源的组织中高度表达,Kindlin-2 在中胚层衍生的组织中高度表达,Kindlin-3 在中胚层和外胚层衍生的组织中高度表达。Kindlins 的失调通常在来自不同器官的癌症中被报道。我们还简要描述了 Kindlins 在其他疾病中的作用。最后,我们分别更新了对 Kindlins 如何被调节和修饰以及 Kindlins 降解机制的最新理解。