PTEN loss in intraductal carcinoma of the prostate has low incidence in Japanese patients

被引:1
作者
Ito, Takanori [1 ]
Takahara, Taishi [1 ]
Taniguchi, Natsuki [1 ]
Yamamoto, Yuki [1 ]
Satou, Akira [1 ]
Ohashi, Akiko [1 ]
Takahashi, Emiko [1 ]
Sassa, Naoto [2 ]
Tsuzuki, Toyonori [1 ]
机构
[1] Aichi Med Univ Hosp, Dept Surg Pathol, 1-1 Yazakokarimata, Nagakute 4801195, Japan
[2] Aichi Med Univ Hosp, Dept Urol, Nagakute, Japan
基金
日本学术振兴会;
关键词
ERG; ethnicity; IDC-P; prostate cancer; PTEN; HIGH-GRADE PIN; NEEDLE-BIOPSY; CANCER; ERG; ADENOCARCINOMA; EXPRESSION; METASTASIS; SPECIMENS; SURVIVAL; FEATURES;
D O I
10.1111/pin.13369
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Clinical and genomic features of prostate cancer (PCa) vary considerably between Asian and Western populations. PTEN loss is the most frequent abnormality in intraductal carcinoma of the prostate (IDC-P) in Western populations. However, its prevalence and significance in Asian populations have not yet been well studied. In the present study, we evaluated PTEN expression in IDC-P in a Japanese population and its association with ERG expression. This study included 45 and 59 patients with PCa with and without IDC-P, respectively, who underwent radical prostatectomy. PTEN loss was observed in 10 patients with PCa with IDC-P (22%) and nine patients with PCa without IDC-P (17%). ERG expression was relatively frequent in patients with PCa with PTEN loss, although a significant difference was not observed. The co-occurrence of PTEN loss and ERG expression was observed in four patients with PCa with IDC-P and one without IDC-P. PTEN loss and ERG expression did not affect progression-free survival, regardless of the presence of IDC-P. The frequency of PTEN loss in IDC-P is lower in Asian patients than in Western patients. Our results indicate that mechanisms underlying IDC-P in Asian populations are different from those of Western populations.
引用
收藏
页码:542 / 548
页数:7
相关论文
共 36 条
[1]   The Molecular Taxonomy of Primary Prostate Cancer [J].
Abeshouse, Adam ;
Ahn, Jaeil ;
Akbani, Rehan ;
Ally, Adrian ;
Amin, Samirkumar ;
Andry, Christopher D. ;
Annala, Matti ;
Aprikian, Armen ;
Armenia, Joshua ;
Arora, Arshi ;
Auman, J. Todd ;
Balasundaram, Miruna ;
Balu, Saianand ;
Barbieri, Christopher E. ;
Bauer, Thomas ;
Benz, Christopher C. ;
Bergeron, Alain ;
Beroukhim, Rameen ;
Berrios, Mario ;
Bivol, Adrian ;
Bodenheimer, Tom ;
Boice, Lori ;
Bootwalla, Moiz S. ;
dos Reis, Rodolfo Borges ;
Boutros, Paul C. ;
Bowen, Jay ;
Bowlby, Reanne ;
Boyd, Jeffrey ;
Bradley, Robert K. ;
Breggia, Anne ;
Brimo, Fadi ;
Bristow, Christopher A. ;
Brooks, Denise ;
Broom, Bradley M. ;
Bryce, Alan H. ;
Bubley, Glenn ;
Burks, Eric ;
Butterfield, Yaron S. N. ;
Button, Michael ;
Canes, David ;
Carlotti, Carlos G. ;
Carlsen, Rebecca ;
Carmel, Michel ;
Carroll, Peter R. ;
Carter, Scott L. ;
Cartun, Richard ;
Carver, Brett S. ;
Chan, June M. ;
Chang, Matthew T. ;
Chen, Yu .
CELL, 2015, 163 (04) :1011-1025
[2]   Aberrant ERG expression cooperates with loss of PTEN to promote cancer progression in the prostate [J].
Carver, Brett S. ;
Tran, Jennifer ;
Gopalan, Anuradha ;
Chen, Zhenbang ;
Shaikh, Safa ;
Carracedo, Arkaitz ;
Alimonti, Andrea ;
Nardella, Caterina ;
Varmeh, Shohreh ;
Scardino, Peter T. ;
Cordon-Cardo, Carlos ;
Gerald, William ;
Pandolfi, Pier Paolo .
NATURE GENETICS, 2009, 41 (05) :619-624
[3]  
Cree IA., 2021, WHO CLASSIFICATION T
[4]   Cribriform architecture prostatic adenocarcinoma in needle biopsies is a strong independent predictor for lymph node metastases in radical prostatectomy [J].
Downes, Michelle R. ;
Xu, Bin ;
van der Kwast, Theodorus H. .
EUROPEAN JOURNAL OF CANCER, 2021, 148 :432-439
[5]   Evaluation of ERG and PTEN protein expression in cribriform architecture prostate carcinomas [J].
Downes, Michelle R. ;
Satturwar, Swati ;
Trudel, Dominique ;
van der Kwast, Theo H. .
PATHOLOGY RESEARCH AND PRACTICE, 2017, 213 (01) :34-38
[6]   Comparative Analysis of Genomic Alterations across Castration Sensitive and Castration Resistant Prostate Cancer via Circulating Tumor DNA Sequencing [J].
Fan, Liancheng ;
Fei, Xiaochen ;
Zhu, Yinjie ;
Pan, Jiahua ;
Sha, Jianjun ;
Chi, Chenfei ;
Gong, Yiming ;
Du, Xinxing ;
Zhou, Lixin ;
Dong, Baijun ;
Xue, Wei .
JOURNAL OF UROLOGY, 2021, 205 (02) :461-469
[7]   Clinical - Pathological comparison of clinical prostate cancer between Japanese Americans in Hawaii and Japanese living in Japan [J].
Fukagai, T ;
Shimada, M ;
Yoshida, H ;
Namiki, T ;
Carlile, RG .
INTERNATIONAL JOURNAL OF ANDROLOGY, 2000, 23 :43-44
[8]   Molecular evidence that invasive adenocarcinoma can mimic prostatic intraepithelial neoplasia (PIN) and intraductal carcinoma through retrograde glandular colonization [J].
Haffner, Michael C. ;
Weier, Christopher ;
Xu, Meng Meng ;
Vaghasia, Ajay ;
Guerel, Bora ;
Guemueskaya, Berrak ;
Esopi, David M. ;
Fedor, Helen ;
Tan, Hsueh-Li ;
Kulac, Ibrahim ;
Hicks, Jessica ;
Isaacs, William B. ;
Lotan, Tamara L. ;
Nelson, William G. ;
Yegnasubramanian, Srinivasan ;
De Marzo, Angelo M. .
JOURNAL OF PATHOLOGY, 2016, 238 (01) :31-41
[9]   Androgen-induced TOP2B-mediated double-strand breaks and prostate cancer gene rearrangements [J].
Haffner, Michael C. ;
Aryee, Martin J. ;
Toubaji, Antoun ;
Esopi, David M. ;
Albadine, Roula ;
Gurel, Bora ;
Isaacs, William B. ;
Bova, G. Steven ;
Liu, Wennuan ;
Xu, Jianfeng ;
Meeker, Alan K. ;
Netto, George ;
De Marzo, Angelo M. ;
Nelson, William G. ;
Yegnasubramanian, Srinivasan .
NATURE GENETICS, 2010, 42 (08) :668-U45
[10]   Atypical Intraductal Cribriform Proliferations of the Prostate Exhibit Similar Molecular and Clinicopathologic Characteristics as Intraductal Carcinoma of the Prostate [J].
Hickman, Richard A. ;
Yu, Hui ;
Li, Jianhong ;
Kong, Max ;
Shah, Rajal B. ;
Zhou, Ming ;
Melamed, Jonathan ;
Deng, Fang-Ming .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2017, 41 (04) :550-556