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胱抑素超家族

Cystatin superfamily.

作者信息

Ochieng Josiah, Chaudhuri Gautam

机构信息

Biochemistry and Cancer Biology, Meharry Medical College, Nashville, TN 37208, USA.

出版信息

J Health Care Poor Underserved. 2010 Feb;21(1 Suppl):51-70. doi: 10.1353/hpu.0.0257.

DOI:10.1353/hpu.0.0257
PMID:20173285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2888135/
Abstract

Cystatins, the classical inhibitors of C1 cysteine proteinases, have been extensively studied and reviewed in the literature. Over the last 20 years, however, proteins containing cystatin domains but lacking protease inhibitory activities have been identified, and most likely more will be described in the near future. These proteins together with family 1, 2, and 3 cystatins constitute the cystatin superfamily. Mounting evidence points to the new roles that some members of the superfamily have acquired over the course of their evolution. This review is focused on the roles of cystatins in: 1) tumorigenesis, 2) stabilization of matrix metalloproteinases, 3) glomerular filtration rate, 4) immunomodulation, and 5) neurodegenerative diseases. It is the goal of this review to get as many investigators as possible to take a second look at the cystatin superfamily regarding their potential involvement in serious human ailments.

摘要

胱抑素是C1半胱氨酸蛋白酶的经典抑制剂,在文献中已得到广泛研究和综述。然而,在过去20年里,已鉴定出含有胱抑素结构域但缺乏蛋白酶抑制活性的蛋白质,而且在不久的将来很可能会描述更多此类蛋白质。这些蛋白质与1、2和3型胱抑素家族一起构成了胱抑素超家族。越来越多的证据表明,该超家族的一些成员在进化过程中获得了新的作用。本综述重点关注胱抑素在以下方面的作用:1)肿瘤发生,2)基质金属蛋白酶的稳定,3)肾小球滤过率,4)免疫调节,以及5)神经退行性疾病。本综述的目的是让尽可能多的研究人员重新审视胱抑素超家族在严重人类疾病中的潜在作用。

相似文献

1
Cystatin superfamily.胱抑素超家族
J Health Care Poor Underserved. 2010 Feb;21(1 Suppl):51-70. doi: 10.1353/hpu.0.0257.
2
Structure/function analysis of human cystatin SN and comparison of the cysteine proteinase inhibitory profiles of human cystatins C and SN.人胱抑素SN的结构/功能分析以及人胱抑素C和SN的半胱氨酸蛋白酶抑制谱比较。
J Dent Res. 1999 Aug;78(8):1401-9. doi: 10.1177/00220345990780080501.
3
Cystatins--inhibitors of cysteine proteinases.胱抑素——半胱氨酸蛋白酶抑制剂。
Crit Rev Oral Biol Med. 1992;3(4):307-32. doi: 10.1177/10454411920030040101.
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Salivary (SD-type) cystatins: over one billion years in the making--but to what purpose?唾液(SD型)半胱氨酸蛋白酶抑制剂:历经十亿多年形成——但目的何在?
Crit Rev Oral Biol Med. 2002;13(6):485-508. doi: 10.1177/154411130201300606.
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Role of cystatins in tumor neovascularization.胱抑素在肿瘤新生血管形成中的作用。
Future Oncol. 2005 Oct;1(5):661-72. doi: 10.2217/14796694.1.5.661.
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Cystatins.胱抑素
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Towards novel anti-cancer strategies based on cystatin function.迈向基于胱抑素功能的新型抗癌策略。
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Friends and relations of the cystatin superfamily--new members and their evolution.胱抑素超家族的朋友与亲属——新成员及其进化
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Epigenetic regulation of cystatins in cancer.癌症中胱抑素的表观遗传调控
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The cystatins: protein inhibitors of cysteine proteinases.胱抑素:半胱氨酸蛋白酶的蛋白质抑制剂。
FEBS Lett. 1991 Jul 22;285(2):213-9. doi: 10.1016/0014-5793(91)80804-c.

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Expression profiles and clinical significance of cystatin family genes in transitional cell carcinoma of the urinary bladder.胱抑素家族基因在膀胱移行细胞癌中的表达谱及临床意义
Bladder (San Franc). 2025 Mar 13;12(1):e21200035. doi: 10.14440/bladder.2024.0057. eCollection 2025.
2
Host-Directed Therapies Based on Protease Inhibitors to Control and HIV Coinfection.基于蛋白酶抑制剂的宿主导向疗法以控制结核与HIV合并感染。
Microorganisms. 2025 Apr 30;13(5):1040. doi: 10.3390/microorganisms13051040.
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Cystatin 6 (CST6) and Legumain (LGMN) are potential mediators in the pathogenesis of preeclampsia.胱抑素6(CST6)和天冬酰胺内肽酶(LGMN)是子痫前期发病机制中的潜在介质。
Sci Rep. 2025 Apr 15;15(1):12945. doi: 10.1038/s41598-025-96823-9.
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evaluation of missense SNPs in cancer-associated Cystatin A protein and their potential to disrupt Cathepsin B interaction.癌症相关胱抑素A蛋白中错义单核苷酸多态性的评估及其破坏组织蛋白酶B相互作用的可能性。
Heliyon. 2025 Feb 5;11(3):e42478. doi: 10.1016/j.heliyon.2025.e42478. eCollection 2025 Feb 15.
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Cystatin from Austrelaps superbus snake venom as a model for identifying potential inhibitors of Trypanosoma cruzi cruzain.来自澳洲棕伊澳蛇蛇毒的胱抑素作为鉴定克氏锥虫克氏蛋白酶潜在抑制剂的模型。
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Exploring proteins within the coccolith matrix.探索颗石藻基质中的蛋白质。
Sci Rep. 2024 Dec 30;14(1):31821. doi: 10.1038/s41598-024-83052-9.
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Unveiling the Roles of Cysteine Proteinases F and W: From Structure to Pathological Implications and Therapeutic Targets.揭示半胱氨酸蛋白酶 F 和 W 的作用:从结构到病理意义及治疗靶点。
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Type 2 Cystatins and Their Roles in the Regulation of Human Immune Response and Cancer Progression.2型胱抑素及其在人类免疫反应调节和癌症进展中的作用。
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本文引用的文献

1
Extracellular proteases as targets for drug development.作为药物开发靶点的细胞外蛋白酶
Curr Protein Pept Sci. 2009 Aug;10(4):297-307. doi: 10.2174/138920309788922207.
2
Reverse dual phase gas diffusion flow injection analysis.反向双相气体扩散流动注射分析
Talanta. 1993 Dec;40(12):1961-6. doi: 10.1016/0039-9140(93)80121-7.
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Aspartic proteases in drug discovery.药物研发中的天冬氨酸蛋白酶
Curr Pharm Des. 2007;13(3):271-85. doi: 10.2174/138161207779313560.
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The serum glycoprotein fetuin-A promotes Lewis lung carcinoma tumorigenesis via adhesive-dependent and adhesive-independent mechanisms.血清糖蛋白胎球蛋白-A通过黏附依赖性和非黏附依赖性机制促进Lewis肺癌的肿瘤发生。
Cancer Res. 2005 Jan 15;65(2):499-506.
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Up-regulation of the extracellular matrix remodeling genes, biglycan, neutrophil gelatinase-associated lipocalin, and matrix metalloproteinase-9 in familial amyloid polyneuropathy.家族性淀粉样多神经病中细胞外基质重塑基因双糖链蛋白聚糖、中性粒细胞明胶酶相关脂质运载蛋白和基质金属蛋白酶-9的上调
FASEB J. 2005 Jan;19(1):124-6. doi: 10.1096/fj.04-2022fje. Epub 2004 Nov 9.
6
Identification of Fetuin-B as a member of a cystatin-like gene family on mouse chromosome 16 with tumor suppressor activity.鉴定胎球蛋白-B为小鼠16号染色体上具有肿瘤抑制活性的类胱抑素基因家族成员。
Genome. 2004 Oct;47(5):931-46. doi: 10.1139/g04-043.
7
Cystatin m: a novel candidate tumor suppressor gene for breast cancer.胱抑素m:一种新的乳腺癌候选肿瘤抑制基因。
Cancer Res. 2004 Oct 1;64(19):6957-64. doi: 10.1158/0008-5472.CAN-04-0819.
8
alpha2HS-glycoprotein, an antagonist of transforming growth factor beta in vivo, inhibits intestinal tumor progression.α2HS糖蛋白是一种体内转化生长因子β的拮抗剂,可抑制肠道肿瘤进展。
Cancer Res. 2004 Sep 15;64(18):6402-9. doi: 10.1158/0008-5472.CAN-04-1117.
9
Annexins expressed on the cell surface serve as receptors for adhesion to immobilized fetuin-A.细胞表面表达的膜联蛋白作为与固定化胎球蛋白A黏附的受体。
Biochim Biophys Acta. 2004 Aug 23;1693(2):111-23. doi: 10.1016/j.bbamcr.2004.06.005.
10
Cystatin C antagonizes transforming growth factor beta signaling in normal and cancer cells.胱抑素C在正常细胞和癌细胞中拮抗转化生长因子β信号传导。
Mol Cancer Res. 2004 Mar;2(3):183-95.