S型半胱氨酸蛋白酶抑制剂对胃肠道肿瘤诊断的研究进展
Research Progress of S-Type Cystatins in the Diagnosis of Gastrointestinal Tumors
DOI: 10.12677/ACM.2022.123306, PDF,   
作者: 王多姿:西安医学院,陕西 西安;何 瑜, 史丽萍:陕西省人民医院消化内二科,陕西 西安
关键词: S型半胱氨酸蛋白酶抑制剂胃癌结直肠癌S-Type Cystatins Gastric Cancer Colorectal Cancer
摘要: S型半胱氨酸蛋白酶抑制剂(S-type Cystatins)是半胱氨酸蛋白酶抑制剂超家族中家族2的成员,包括半胱氨酸蛋白酶抑制剂SN、SA以及S,在胃肠道恶性肿瘤的生长、侵袭转移等病理过程中发挥重要作用,并且S-type Cystatins在肿瘤组织中的表达水平与肿瘤的生长、侵袭转移程度及预后相关,有望成为新型的胃肠道肿瘤诊断分子标志物。本文就半胱氨酸蛋白酶抑制剂的分类、在肿瘤发生发展中的作用以及S型半胱氨酸蛋白酶抑制剂在胃肠道肿瘤诊断中的价值作一综述。
Abstract: S-type Cystatin is a member of family 2 in the Cystatins Superfamily, including SN, SA and S, which play an important role in the growth, invasion and metastasis of gastrointestinal tumors. The expression level of S-type Cystatin in tumor tissue is related to the growth, invasion, metastasis and prognosis of tumor, which is expected to become a new molecular marker for the diagnosis of gastrointestinal tumors. This article reviews the classification, structure, role of cystatins in tumor development and the value of S-type Cystatins in diagnosis of gastrointestinal tumors.
文章引用:王多姿, 何瑜, 史丽萍. S型半胱氨酸蛋白酶抑制剂对胃肠道肿瘤诊断的研究进展[J]. 临床医学进展, 2022, 12(3): 2131-2136. https://doi.org/10.12677/ACM.2022.123306

参考文献

[1] Bray, F., Ferlay, J., Soerjomataram, I., Siegel, R.L., Torre, L.A. and Jemal, A. (2018) Global Cancer Statistics 2018: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA: A Cancer Journal for Clinicians, 68, 394-424. [Google Scholar] [CrossRef] [PubMed]
[2] 袁思依, 李景南. 分子标志物在结直肠癌筛查中的应用[J]. 中国实用内科杂志, 2018, 38(9): 788-791.
[3] Fossum, K. and Whitaker, J.R. (1968) Ficin and Papain Inhibitor from Chicken Egg White. Archives of Biochemistry and Biophysics, 125, 367-375. [Google Scholar] [CrossRef] [PubMed]
[4] Anastasi, A., Brown, M.A., Kembhavi, A.A., Nicklin, M.J.H., Sayers, C.A., Sunter, D.C., et al. (1983) Cystatin, a Protein Inhibitor of Cysteine Proteinases. Improved Purification from Egg White, Characterization, and Detection in Chicken Serum. Biochemical Journal, 211, 129-138. [Google Scholar] [CrossRef] [PubMed]
[5] Shamsi, A. and Bano, B. (2017) Journey of Cystatins from Being Merethiol Protease Inhibitors to at Heart of Many Pathological Conditions. International Journal of Biological Macromolecules, 102, 674-693. [Google Scholar] [CrossRef] [PubMed]
[6] Abrahamson, M., Barrett, A.J., Salvesen, G. and Grubb, A. (1986) Isolation of Six Cysteine Proteinase Inhibitors from Human Urine. Their Physicochemical and Enzyme Kinetic Properties and Concentrations in Biological Fluids. Journal of Biological Chemistry, 261, 11282-11289. [Google Scholar] [CrossRef
[7] Ni, J., Abrahamson, M., Zhang, M., Fernandez, M.A., Grubb, A., Su, J., et al. (1997) Cystatin E Is a Novel Human Cysteine Proteinase Inhibitor with Structural Resemblance to Family 2 Cystatins. Journal of Biological Chemistry, 272, 10853-10858. [Google Scholar] [CrossRef] [PubMed]
[8] Ni, J., Fernandez, M.A., Danielsson, L., Chillakuru, R.A., Zhang, J., Grubb, A., et al. (1998) Cystatin F Is a Glycosylated Human Low Molecular Weight Cysteine Proteinase Inhibitor. Journal of Biological Chemistry, 273, 24797-24804. [Google Scholar] [CrossRef] [PubMed]
[9] Hook, V., Funkelstein, L., Wegrzyn, J., Bark, S., Kindy, M. and Hook, G. (2012) Cysteine Cathepsins in the Secretory Vesicle Produce Active Peptides: Cathepsin L Generates Peptide Neurotransmitters and Cathepsin B Produces Beta-Amyloid of Alzheimer’s Disease. Biochimica et Biophysica Acta (BBA)—Proteins and Proteomics, 1824, 89-104. [Google Scholar] [CrossRef] [PubMed]
[10] Cheng, X.W., Huang, Z., Kuzuya, M., Okumura, K. and Murohara, T. (2011) Cysteine Protease Cathepsins in Atherosclerosis-Based Vascular Disease and Its Complications. Hypertension, 58, 978-986. [Google Scholar] [CrossRef
[11] Harlozinska, A. (2005) Progress in Molecular Mechanisms of Tumor Metastasis and Angiogenesis. Anticancer Research, 25, 3327-3333.
[12] Satoko, I., Eiichi, S. and Kazuo, S. (1984) Isolation and Amino Acid Sequence of SAP-1, an Acidic Protein of Human Whole Saliva, and Sequence Homology with Human Gamma-Trace. Journal of Biochemistry, 96, 489-498. [Google Scholar] [CrossRef] [PubMed]
[13] Isemura, S., Saitoh, E. and Sanada, K. (1986) Characterization of a New Cysteine Proteinase Inhibitor of Human Saliva, Cystatin SN, Which Is Immunologically Related to Cystatin S. FEBS Letters, 198, 14514-14519. [Google Scholar] [CrossRef] [PubMed]
[14] Isemura, S., Saitoh, E. and Sanada, K. (1987) Characterization and Amino Acid Sequence of a New Acidic Cysteine Proteinase Inhibitor (Cystatin SA) Structurally Closely Related to Cystatin S, from Human Whole Saliva. Journal of Biochemistry, 102, 693-704. [Google Scholar] [CrossRef] [PubMed]
[15] Saitoh, E., Kim, H.S., Smithies, O. and Maeda, N. (1987) Human Cysteine-Proteinase Inhibitors: Nucleotide Sequence Analysis of Three Members of the Cystatin Gene Family. Gene, 61, 329-338. [Google Scholar] [CrossRef
[16] Bobek, L.A., Aguirre, A. and Levine, M.J. (1991) Human Salivary Cystatin S. Cloning, Sequence Analysis, Hybridization in Situ and Immunocytochemistry. Biochemical Journal, 278, 627-635. [Google Scholar] [CrossRef] [PubMed]
[17] Dickinson, D.P., Thiesse, M. and Hicks, M.J. (2002) Expression of Type 2 Cystatin Genes CST1-CST5 in Adult Human Tissues and the Developing Submandibular Gland. DNA and Cell Biology, 21, 47-65. [Google Scholar] [CrossRef] [PubMed]
[18] Choi, E.H., Kim, J.T., Kim, J.H., Kim, S.Y., Song, E.Y., Kim, J.W., et al. (2009) Upregulation of the Cysteine Protease Inhibitor, Cystatin SN, Contributes to Cell Proliferation and Cathepsin Inhibition in Gastric Cancer. Clinica Chimica Acta, 406, 45-51. [Google Scholar] [CrossRef] [PubMed]
[19] Yoneda, K., Iida, H., Endo, H., Hosono, K., Akiyama, T., Takahashi, H., et al. (2009) Identification of Cystatin SN as a Novel Tumor Marker for Colorectal Cancer. International Journal of Oncology, 35, 33-40. [Google Scholar] [CrossRef
[20] Kim, J.T., Lee, S.J., Kang, M.A., Park, J.E., Kim, B.Y., Yoon, D.Y., et al. (2013) Cystatin SN Neutralizes the Inhibitory Effect of Cystatin C on Cathepsin B Activity. Cell Death & Disease, 4, Article No. e974. [Google Scholar] [CrossRef] [PubMed]
[21] Zhang, W.P., Wang, Y., Tan, D. and Xing, C.G. (2020) Cystatin 2 Leads to a Worse Prognosis in Patients with Gastric Cancer. Journal of Biological Regulators and Homeostatic Agents, 34, 2059-2067.
[22] Wang, Z., Chen, G., Wang, Q., Lu, W. and Xu, M. (2017) Identification and Validation of a Prognostic 9-Genes Expression Signature for Gastric Cancer. Oncotarget, 8, 73826-73836. [Google Scholar] [CrossRef] [PubMed]
[23] Wang, Q., Wen Y G., Li, D.P., Xia, J., Zhou, C.Z., Yan, D.W., et al. (2012) Upregulated INHBA Expression Is Associated with Poor Survival in Gastric Cancer. Medical Oncology, 29, 77-83.
[24] Cui, J., Chen, Y., Chou W C., Sun, L., Chen, L., Suo, J., et al. (2011) An Integrated Transcriptomic and Computational Analysis for Biomarker Identification in Gastric Cancer. Nucleic Acids Research, 39, 1197-1207. [Google Scholar] [CrossRef] [PubMed]
[25] Yi, Q.Z., Jing, J.Z., Hong, J.S. and Li, D.W. (2017) Overexpression of CST4 Promotes Gastric Cancer Aggressiveness by Activating the ELFN2 Signaling Pathway. American Journal of Cancer Research, 7, 2290-2304.
[26] Dou, Y.L., Lyu, Y.L., Zhou, X.J., He, L.F., Liu, L.H., Li, P.F., et al. (2018) Antibody-Sandwich Elisa Analysis of a Novel Blood Biomarker of CST4 in Gastrointestinal Cancers. OncoTargets and Therapy, 11, 1743-1756. [Google Scholar] [CrossRef
[27] 吴明兰, 林美花, 翟优, 吕朵, 张乔, 吴国兰, 等. 半胱氨酸蛋白酶抑制剂S在胃肠癌中的诊断价值研究[J]. 中国临床药理学杂志, 2021, 37(5): 503-506.