» Articles » PMID: 35223512

SPINKs in Tumors: Potential Therapeutic Targets

Overview
Journal Front Oncol
Specialty Oncology
Date 2022 Feb 28
PMID 35223512
Authors
Affiliations
Soon will be listed here.
Abstract

The serine protease inhibitor Kazal type (SPINK) family includes SPINK1-14 and is the largest branch in the serine protease inhibitor family. SPINKs play an important role in pancreatic physiology and disease, sperm maturation and capacitation, Nager syndrome, inflammation and the skin barrier. Evidence shows that the unregulated expression of SPINK1, 2, 4, 5, 6, 7, and 13 is closely related to human tumors. Different SPINKs exhibit various regulatory modes in different tumors and can be used as tumor prognostic markers. This article reviews the role of SPINK1, 2, 4, 5, 6, 7, and 13 in different human cancer processes and helps to identify new cancer treatment targets.

Citing Articles

Crosstalk of Expression With Patient Mortality, Immunotherapy and Metastasis in Pan-Cancer Based on Integrated Multi-Omics Analyses.

Cao X, Luo N, Liu X, Guo K, Deng M, Lv C Onco Targets Ther. 2025; 18:161-177.

PMID: 39926372 PMC: 11806753. DOI: 10.2147/OTT.S487126.


Activation of cellular responses by cyclic dinucleotides and lipopolysaccharide: a proteomic study on gingival fibroblasts.

Elmanfi S, Onyedibe K, Aryal U, Kononen E, Sintim H, Gursoy U J Oral Microbiol. 2024; 17(1):2431453.

PMID: 39669221 PMC: 11632945. DOI: 10.1080/20002297.2024.2431453.


SPINK13 acts as a tumor suppressor in hepatocellular carcinoma by inhibiting Akt phosphorylation.

Lun Y, Sun J, Wei L, Liu B, Li Z, Dong W Cell Death Dis. 2024; 15(11):822.

PMID: 39537605 PMC: 11561306. DOI: 10.1038/s41419-024-07214-3.


The microprotein HDSP promotes gastric cancer progression through activating the MECOM-SPINK1-EGFR signaling axis.

Chen Y, Li Q, Yu X, Lu L, Zhou Z, Li M Nat Commun. 2024; 15(1):8381.

PMID: 39333095 PMC: 11437185. DOI: 10.1038/s41467-024-50986-7.


Therapeutic potential of the secreted Kazal-type serine protease inhibitor SPINK4 in colitis.

Wang Y, Han J, Yang G, Zheng S, Zhou G, Liu X Nat Commun. 2024; 15(1):5874.

PMID: 38997284 PMC: 11245600. DOI: 10.1038/s41467-024-50048-y.


References
1.
Borgono C, Michael I, Komatsu N, Jayakumar A, Kapadia R, Clayman G . A potential role for multiple tissue kallikrein serine proteases in epidermal desquamation. J Biol Chem. 2006; 282(6):3640-52. DOI: 10.1074/jbc.M607567200. View

2.
Di W, Hennekam R, Callard R, Harper J . A heterozygous null mutation combined with the G1258A polymorphism of SPINK5 causes impaired LEKTI function and abnormal expression of skin barrier proteins. Br J Dermatol. 2009; 161(2):404-12. DOI: 10.1111/j.1365-2133.2009.09231.x. View

3.
Weber C, Fischer J, Redelfs L, Rademacher F, Harder J, Weidinger S . The serine protease inhibitor of Kazal-type 7 (SPINK7) is expressed in human skin. Arch Dermatol Res. 2017; 309(9):767-771. DOI: 10.1007/s00403-017-1773-9. View

4.
Yan R, Zhu T, Wang Q, Yang K, Li J, Guan S . Increased Serum Levels of Trypsin Inhibitor Kazal1 in Patients with HBV-Related Hepatocellular Carcinoma Predict a Poor Prognosis. Clin Lab. 2021; 67(1). DOI: 10.7754/Clin.Lab.2020.200411. View

5.
Redelfs L, Fischer J, Weber C, Wu Z, Meyer-Hoffert U . The serine protease inhibitor of Kazal-type 9 (SPINK9) is expressed in lichen simplex chronicus, actinic keratosis and squamous cell carcinoma. Arch Dermatol Res. 2016; 308(2):133-7. DOI: 10.1007/s00403-015-1616-5. View