دورية أكاديمية
Cathepsins mediate tumor metastasis.
| العنوان: | Cathepsins mediate tumor metastasis. |
|---|---|
| المؤلفون: | Tan GJ; Gong-Jun Tan, Fa-Qing Tang, Department of Clinical Laboratory, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China., Peng ZK, Lu JP, Tang FQ |
| المصدر: | World journal of biological chemistry [World J Biol Chem] 2013 Nov 26; Vol. 4 (4), pp. 91-101. |
| نوع المنشور: | Journal Article; Review |
| اللغة: | English |
| بيانات الدورية: | Publisher: Baishideng Publishing Group Country of Publication: United States NLM ID: 101546471 Publication Model: Print Cited Medium: Print ISSN: 1949-8454 (Print) Linking ISSN: 19498454 NLM ISO Abbreviation: World J Biol Chem Subsets: PubMed not MEDLINE |
| أسماء مطبوعة: | Publication: 2014- : Pleasanton, CA : Baishideng Publishing Group Original Publication: Hong Kong : Baishideng Publishing Group |
| مستخلص: | Cathepsins are highly expressed in various human cancers, associated with tumor metastasis. It is superfamily, concluding A, B, C, D, E, F, G, H, L, K, O, S, V, and W family members. As a group of lysosomal proteinases or endopeptidases, each member has a different function, playing different roles in distinct tumorigenic processes such as proliferation, angiogenesis, metastasis, and invasion. Cathepsins belong to a diverse number of enzyme subtypes, including cysteine proteases, serine proteases and aspartic proteases. The contribution of cathepsins to invasion in human cancers is well documented, although the precise mechanisms by which cathepsins exert their effects are still not clear. In the present review, the role of cathepsin family members in cancer is discussed. |
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| فهرسة مساهمة: | Keywords: Cathepsin; Mechanism; Metastasis; Tumor |
| تواريخ الأحداث: | Date Created: 20131217 Date Completed: 20140624 Latest Revision: 20220419 |
| رمز التحديث: | 20231215 |
| مُعرف محوري في PubMed: | PMC3856311 |
| DOI: | 10.4331/wjbc.v4.i4.91 |
| PMID: | 24340132 |
| قاعدة البيانات: | MEDLINE |
| تدمد: | 1949-8454 |
|---|---|
| DOI: | 10.4331/wjbc.v4.i4.91 |