Kallikrein 5 overexpression is associated with poor prognosis in uterine cervical cancer

被引:10
作者
Chang, Jee Suk [1 ]
Kim, Nalee [2 ]
Kim, Ji-Ye [3 ]
Do, Sung-Im [4 ]
Cho, Yeona [5 ]
Kim, Hyun Soo [6 ]
Kim, Yong Bae [1 ]
机构
[1] Yonsei Univ, Yonsei Canc Ctr, Dept Radiat Oncol, Coll Med, 50-1 Yonsei Ro, Seoul 03722, South Korea
[2] Sungkyunkwan Univ, Samsung Med Ctr, Dept Radiat Oncol, Sch Med, Seoul, South Korea
[3] Inje Univ, Ilsan Paik Hosp, Dept Pathol, Goyang, South Korea
[4] Sungkyunkwan Univ, Kangbuk Samsung Hosp, Dept Pathol, Sch Med, Seoul, South Korea
[5] Yonsei Univ, Gangnam Severance Hosp, Dept Radiat Oncol, Coll Med, Seoul, South Korea
[6] Sungkyunkwan Univ, Samsung Med Ctr, Dept Pathol & Translat Genom, Sch Med, 81 Irwon Ro, Seoul 06351, South Korea
关键词
Uterine Cervical Cancer; Kallikreins; Radiation Therapy; Prognosis; PROTEINASE-ACTIVATED RECEPTORS; PEPTIDASES; CHEMORADIOTHERAPY; EXPRESSION;
D O I
10.3802/jgo.2020.31.e78
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Kallikrein 5 (KLK5), which is frequently observed in normal cervico-vaginal fluid, is known to be related to prognosis in several solid tumors. We investigated the prognostic significance of KLK5 in uterine cervical cancer using tumor tissue microarray and immunohistochemistry staining. Methods: We analyzed samples of165 patients with uterine cervical cancer who received definitive radiation therapy between 2004 and 2012. We divided patients into two groups stratified by their KLK5 activity by immunohistochemistry staining: negative/weak (0-1+) (n=120 patients) and moderate/strong (2-3+) group (n=45 patients). Patient and tumor characteristics, patterns of failure, and survival outcomes were compared. Univariable and multivariable analyses were performed to identify prognostic factors. Results: Patients with KLK5 2-3+ were younger (median: 52 vs. 60 years) and had frequent paraaortic lymph node involvement (40.0% vs. 18.3%) than those with KLK5 0-1+. With a median follow-up of 60.8 (interquartile range, 47.5-77.9) months, patients with KLK5 2-3+ had inferior 5-year locoregional recurrence-free survival and distant metastasis-free survival of 61.7% (vs. 77.5% in KLK5 0-1+ group) and 59.4% (vs. 72.8% in the KLK5 0-1+ group), respectively (all p<0.05). KLK5 2-3+ expression retained its significance after adjusting for other well-known prognostic factors of tumor size and stage in multivariable analysis. Conclusions: KLK5 overexpression is associated with the aggressiveness of cervical cancer and may underlie the diminished response to conventional treatments. Therefore, KLK5 could be a reliable prognostic factor in cervical cancer.
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页码:1 / 11
页数:11
相关论文
共 39 条
[1]   Kallikrein-related peptidase genes as promising biomarkers for prognosis and monitoring of human malignancies [J].
Avgeris, Margaritis ;
Mavridis, Konstantinos ;
Scorilas, Andreas .
BIOLOGICAL CHEMISTRY, 2010, 391 (05) :505-511
[2]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[3]   Degradation of corneodesmosome proteins by two serine proteases of the kallikrein family, SCTE/KLK5/hK5 and SCCE/KLK7/hK7 [J].
Caubet, C ;
Jonca, N ;
Brattsand, M ;
Guerrin, M ;
Bernard, D ;
Schmidt, R ;
Egelrud, T ;
Simon, M ;
Serre, G .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2004, 122 (05) :1235-1244
[4]   Kallikrein-related peptidases targeted therapies in prostate cancer: perspectives and challenges [J].
Cereda, Vittore ;
Formica, Vincenzo ;
Menghi, Antonello ;
Pellicori, Stefania ;
Roselli, Mario .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2015, 24 (07) :929-947
[5]   Tumor-related leukocytosis is associated with poor radiation response and clinical outcome in uterine cervical cancer patients [J].
Cho, Y. ;
Kim, K. H. ;
Yoon, H. I. ;
Kim, G. E. ;
Kim, Y. B. .
ANNALS OF ONCOLOGY, 2016, 27 (11) :2067-2074
[6]   In Situ Normoxia Enhances Survival and Proliferation Rate of Human Adipose Tissue-Derived Stromal Cells without Increasing the Risk of Tumourigenesis [J].
Choi, Jane Ru ;
Pingguan-Murphy, Belinda ;
Abas, Wan Abu Bakar Wan ;
Yong, Kar Wey ;
Poon, Chi Tat ;
Azmi, Mat Adenan Noor ;
Omar, Siti Zawiah ;
Chua, Kien Hui ;
Xu, Feng ;
Safwani, Wan Kamarul Zaman Wan .
PLOS ONE, 2015, 10 (01)
[7]  
Dhar S, 2001, CLIN CANCER RES, V7, P3393
[8]   Circulating biomarker tissue kallikrein-related peptidase KLK5 impacts ovarian cancer patients' survival [J].
Dorn, J. ;
Magdolen, V. ;
Gkazepis, A. ;
Gerte, T. ;
Harlozinska, A. ;
Sedlaczek, P. ;
Diamandis, E. P. ;
Schuster, T. ;
Harbeck, N. ;
Kiechle, M. ;
Schmitt, M. .
ANNALS OF ONCOLOGY, 2011, 22 (08) :1783-1790
[9]   Kallikrein-related peptidases (KLKs) and the hallmarks of cancer [J].
Filippou, Panagiota S. ;
Karagiannis, George S. ;
Musrap, Natasha ;
Diamandis, Eleftherios P. .
CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 2016, 53 (04) :277-291
[10]   Targeting MET in cancer: rationale and progress [J].
Gherardi, Ermanno ;
Birchmeier, Walter ;
Birchmeier, Carmen ;
Woude, George Vande .
NATURE REVIEWS CANCER, 2012, 12 (02) :89-103