HtrA1, a potential predictor of response to cisplatin-based combination chemotherapy in gastric cancer

被引:21
作者
Catalano, Vincenzo
Mellone, Pasquale [1 ]
d'Avino, Alfredo [1 ]
Shridhar, Viji [2 ]
Staccioli, Maria Pia [3 ]
Graziano, Francesco
Giordani, Paolo
Rossi, David
Baldelli, Anna Maria
Alessandroni, Paolo
Santini, Daniele
Lorenzon, Laura [4 ]
Testa, Enrica [5 ]
D'Emidio, Silvia
De Nictolis, Michele [3 ]
Muretto, Pietro [3 ]
Fedeli, Stefano Luzi
Baldi, Alfonso [1 ]
机构
[1] Univ Naples 2, Dept Biochem, Pathol Sect, I-80138 Naples, Italy
[2] Mayo Clin, Dept Lab Med & Expt Pathol, Ctr Canc, Rochester, MN USA
[3] Azienda Osped Osped San Salvatore, Dept Histopathol, Pesaro, Italy
[4] Univ Roma La Sapienza, Dept Surg A, Fac Med 2, Rome, Italy
[5] Urbino Hosp, Urbino, Italy
关键词
chemoresistance; chemotherapy; cisplatin; gastric cancer; HtrA1; SERINE-PROTEASE HTRA1; ITALIAN GROUP; PHASE-II; RESISTANCE; FLUOROURACIL; EXPRESSION; DOCETAXEL; REPAIR;
D O I
10.1111/j.1365-2559.2011.03818.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: HtrA1 is a member of the HtrA (high-temperature requirement factor A) family of serine proteases. HtrA1 plays a protective role in various malignancies due to its tumour suppressive properties. The aim of this study was to determine HtrA1 expression as a predictor of chemoresponse in patients with advanced gastric cancer. Methods and results: HtrA1 expression was determined by immunohistochemistry on specimens of primary gastric cancer from 80 patients treated consecutively with cisplatin-based combination chemotherapy. Response to chemotherapy was assessed according to Response Evaluation Criteria in Solid Tumours (RECIST) criteria. Our population consisted of males/females [51/29; median age 64 years (range 32-82)]. A complete or partial response was observed in 71.4% [95% confidence interval (CI) 54.7-88.2], 66.7% (95% CI 47.8-85.5) and 28.6% (95 CI 11.8-45.3) of tumours showing high, medium and low HtrA1 expression, respectively. A statistically significant association between HtrA1 expression and the clinical response was observed (P = 0.002). The median overall survival for patients with high/medium expression was 17 months compared to 9.5 months for patients with low HtrA1 expression (P = 0.037). Conclusions: Identification of HtrA1 in gastric cancer prior to chemotherapy indicates that levels of HtrA1 could be used to predict response to platinum-based combination therapies. Further assessment of HtrA1 expression is highly warranted in large, prospective studies.
引用
收藏
页码:669 / 678
页数:10
相关论文
共 38 条
[1]  
Aebi S, 1996, CANCER RES, V56, P3087
[2]  
[Anonymous], 2009, J CLIN ONCOL S
[3]  
[Anonymous], J CLIN ONCOL S18
[4]   The HtrA1 serine protease is down-regulated during human melanoma progression and represses growth of metastatic melanoma cells [J].
Baldi, A ;
De Luca, A ;
Morini, M ;
Battista, T ;
Felsani, A ;
Baldi, F ;
Catricalà, C ;
Amantea, A ;
Noonan, DM ;
Albini, A ;
Natali, PG ;
Lombardi, D ;
Paggi, MG .
ONCOGENE, 2002, 21 (43) :6684-6688
[5]   The serine protease HtrA1 is a novel prognostic factor for human mesothelioma [J].
Baldi, Alfonso ;
Mottolese, Marcella ;
Vincenzi, Bruno ;
Campioni, Mara ;
Mellone, Pasquale ;
Di Marino, Mariapia ;
di Crescenzo, Vincenzo G. ;
Visca, Paolo ;
Menegozzo, Simona ;
Spugnini, Enrico P. ;
Citro, Gennaro ;
Ceribelli, Anna ;
Mirri, Alessandra ;
Chien, Jereiny ;
Shridhar, Viji ;
Ehrmann, Michael ;
Santini, Mario ;
Facciolo, Francesco .
PHARMACOGENOMICS, 2008, 9 (08) :1069-1077
[6]   Fluorouracil versus combination of irinotecan plus cisplatin versus S-1 in metastatic gastric cancer: a randomised phase 3 study [J].
Boku, Narikazu ;
Yamamoto, Seiichiro ;
Fukuda, Haruhiko ;
Shirao, Kuniaki ;
Doi, Toshihiko ;
Sawaki, Akira ;
Koizumi, Wasaburo ;
Saito, Hiroshi ;
Yamaguchi, Kensei ;
Takiuchi, Hiroya ;
Nasu, Junichiro ;
Ohtsu, Atsushi .
LANCET ONCOLOGY, 2009, 10 (11) :1063-1069
[7]   How do real tumors become resistant to cisplatin? [J].
Borst, Piet ;
Rottenberg, Sven ;
Jonkers, Jos .
CELL CYCLE, 2008, 7 (10) :1353-1359
[8]   Intensive weekly chemotherapy for advanced gastric cancer using fluorouracil, cisplatin, epi-doxorubicin, 6S-leucovorin, glutathione, and filgrastim: A report from the Italian group for the study of digestive tract cancer [J].
Cascinu, S ;
Labianca, R ;
Alessandroni, P ;
Marcellini, M ;
Silva, RR ;
Pancera, G ;
Testa, E ;
Martignoni, G ;
Barni, S ;
Frontini, L ;
Zaniboni, A ;
Luporini, G ;
Cellerino, R ;
Catalano, G .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (11) :3313-3319
[9]   Pegylated liposomal doxorubicin, 5-fluorouracil and cisplatin versus mitomycin-C, 5-fluorouracil and cisplatin for advanced gastric cancer: A randomised phase II trial [J].
Cascinu, S. ;
Labianca, R. ;
Catalano, V. ;
Ferrau, F. ;
Pucci, F. ;
Silva, R. R. ;
Luppi, G. ;
Berardi, R. ;
Beretta, G. D. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (15)
[10]   Infusional 5-fluorouracil, cisplatin and mitomycin C in advanced gastric cancer: A low cost effective regimen [J].
Cascinu, S ;
Baldelli, AM ;
Catalano, V ;
Giordani, P ;
Beretta, GD ;
Silva, RR ;
Gasparini, G ;
Mari, D ;
Maisano, R ;
Salvagni, S ;
Barni, S ;
Labianca, R ;
Frontini, L ;
Curti, C ;
Catalano, G .
BRITISH JOURNAL OF CANCER, 2002, 86 (02) :213-217