Literature DB >> 29164703

Clinicopathological characteristics of patients with upper urinary tract urothelial cancer with loss of immunohistochemical expression of the DNA mismatch repair proteins in universal screening.

Shinji Urakami1,2, Naoko Inoshita3, Suguru Oka1, Yu Miyama3, Sachio Nomura4, Masami Arai4, Kazushige Sakaguchi1, Kazuhiro Kurosawa1, Toshikazu Okaneya1.   

Abstract

OBJECTIVES: To assess the detection rate of putative Lynch syndrome-associated upper urinary tract urothelial cancer among all upper urinary tract urothelial cancers and to examine its clinicopathological characteristics.
METHODS: A total of 143 patients with upper urinary tract urothelial cancer who had received total nephroureterectomy were immunohistochemically stained for the expression of mismatch repair proteins MLH1, PMS2, MSH2 and MSH6. For all suspected mismatch repair-deficient cases, MMR genetic testing was recommended and clinicopathological features were examined.
RESULTS: Loss of mismatch repair proteins was found in seven patients (5%) who were thus categorized as putative Lynch syndrome-associated upper urinary tract urothelial cancer. Five of these patients showed dual loss of MSH2/MSH6. Two patients were confirmed to be MSH2 germline mutation carriers. Histologically, all seven tumors were low-grade atypical urothelial carcinoma and showed its unique histological features, such as an inverted papilloma-like growth pattern and a villous to papillary structure with mild stratification of tumor cells. Six tumors had no invasion of the muscularis propria. No recurrence or cancer-related deaths were reported in these seven patients. Just three patients met the revised Amsterdam criteria.
CONCLUSIONS: This is the first report that universally examined mismatch repair immunohistochemical screening for upper urinary tract urothelial cancers. The prevalence (5%) of putative Lynch syndrome-associated upper urinary tract urothelial cancers is much higher than we had expected. We ascertained that putative Lynch syndrome-associated upper urinary tract urothelial cancers were clinically in the early stage and histologically classified into low-grade malignancy with its characteristic pathological features. The clinicopathological characteristics that we found in the present study could become additional possible markers in the diagnosis of Lynch syndrome-associated upper urinary tract urothelial cancers.
© 2017 The Japanese Urological Association.

Entities:  

Keywords:  DNA mismatch repair proteins; Lynch syndrome; immunohistochemistry; universal screening; upper urinary tract cancer

Mesh:

Substances:

Year:  2017        PMID: 29164703     DOI: 10.1111/iju.13481

Source DB:  PubMed          Journal:  Int J Urol        ISSN: 0919-8172            Impact factor:   3.369


  9 in total

1.  Identification of Lynch syndrome-associated DNA mismatch repair-deficient bladder cancer in a Japanese hospital-based population.

Authors:  Makoto Kagawa; Satoru Kawakami; Azusa Yamamoto; Okihide Suzuki; Nao Kamae; Hidetaka Eguchi; Yasushi Okazaki; Gou Yamamoto; Kiwamu Akagi; Jun-Ichi Tamaru; Tatsuro Yamaguchi; Tomio Arai; Hideyuki Ishida
Journal:  Int J Clin Oncol       Date:  2021-07-02       Impact factor: 3.402

2.  Systematic Review: An Update on the Spectrum of Urological Malignancies in Lynch Syndrome.

Authors:  Dora Huang; Surena F Matin; Nathan Lawrentschuk; Morgan Roupret
Journal:  Bladder Cancer       Date:  2018-07-30

Review 3.  Lynch Syndrome: Its Impact on Urothelial Carcinoma.

Authors:  Andrea Katharina Lindner; Gert Schachtner; Gennadi Tulchiner; Martin Thurnher; Gerold Untergasser; Peter Obrist; Iris Pipp; Fabian Steinkohl; Wolfgang Horninger; Zoran Culig; Renate Pichler
Journal:  Int J Mol Sci       Date:  2021-01-07       Impact factor: 5.923

Review 4.  How Should We Test for Lynch Syndrome? A Review of Current Guidelines and Future Strategies.

Authors:  Richard Gallon; Peter Gawthorpe; Rachel L Phelps; Christine Hayes; Gillian M Borthwick; Mauro Santibanez-Koref; Michael S Jackson; John Burn
Journal:  Cancers (Basel)       Date:  2021-01-22       Impact factor: 6.639

Review 5.  Diagnosis of Lynch Syndrome and Strategies to Distinguish Lynch-Related Tumors from Sporadic MSI/dMMR Tumors.

Authors:  Julie Leclerc; Catherine Vermaut; Marie-Pierre Buisine
Journal:  Cancers (Basel)       Date:  2021-01-26       Impact factor: 6.639

6.  Morphological predictors for microsatellite instability in urothelial carcinoma.

Authors:  Eduardo Sobrino-Reig; Telma Meizoso; Jesús García; David Varillas-Delgado; Yasmina B Martin
Journal:  Diagn Pathol       Date:  2021-11-20       Impact factor: 2.644

7.  Identification of Germline Mutations in Upper Tract Urothelial Carcinoma With Suspected Lynch Syndrome.

Authors:  Bao Guan; Jie Wang; Xuesong Li; Lin Lin; Dong Fang; Wenwen Kong; Chuangyu Tian; Juan Li; Kunlin Yang; Guanpeng Han; Yucai Wu; Yuhui He; Yiji Peng; Yanfei Yu; Qun He; Shiming He; Yanqing Gong; Liqun Zhou; Qi Tang
Journal:  Front Oncol       Date:  2022-03-16       Impact factor: 6.244

8.  Detection of Microsatellite Instability in Colonoscopic Biopsies and Postal Urine Samples from Lynch Syndrome Cancer Patients Using a Multiplex PCR Assay.

Authors:  Rachel Phelps; Richard Gallon; Christine Hayes; Eli Glover; Philip Gibson; Ibrahim Edidi; Tom Lee; Sarah Mills; Adam Shaw; Rakesh Heer; Angela Ralte; Ciaron McAnulty; Mauro Santibanez-Koref; John Burn; Michael S Jackson
Journal:  Cancers (Basel)       Date:  2022-08-08       Impact factor: 6.575

Review 9.  Microsatellite Instability: From the Implementation of the Detection to a Prognostic and Predictive Role in Cancers.

Authors:  Martina Amato; Renato Franco; Gaetano Facchini; Raffaele Addeo; Fortunato Ciardiello; Massimiliano Berretta; Giulia Vita; Alessandro Sgambato; Sandro Pignata; Michele Caraglia; Marina Accardo; Federica Zito Marino
Journal:  Int J Mol Sci       Date:  2022-08-05       Impact factor: 6.208

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.