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Recurrent WWTR1 S89W mutations and Hippo pathway deregulation in clear cell carcinomas of the cervix

Authors :
Sarah H Kim
Thais Basili
Higinio Dopeso
Arnaud Da Cruz Paula
Rui Bi
Shirin Issa Bhaloo
Fresia Pareja
Qing Li
Edaise M da Silva
Yingjie Zhu
Timothy Hoang
Pier Selenica
Rajmohan Murali
Eric Chan
Michelle Wu
Fatemeh Derakhshan
Ana Maroldi
Etta Hanlon
Carlos Gil Ferreira
Jose Roberto Lapa e Silva
Nadeem R Abu‐Rustum
Dmitriy Zamarin
Sarat Chandarlapaty
Cathleen Matrai
Ju‐Yoon Yoon
Jorge S Reis‐Filho
Kay J Park
Britta Weigelt
Source :
The Journal of pathologyReferences. 257(5)
Publication Year :
2022

Abstract

Clear cell carcinoma (CCC) of the cervix (cCCC) is a rare and aggressive type of human papillomavirus (HPV)-negative cervical cancer with limited effective treatment options for recurrent or metastatic disease. Historically, CCCs of the lower genital tract were associated with in utero diethylstilbestrol exposure; however, the genetic landscape of sporadic cCCCs remains unknown. Here we sought to define the molecular underpinning of cCCCs. Using a combination of whole-exome, targeted capture, and RNA-sequencing, we identified pathogenic genetic alterations in the Hippo signaling pathway in 50% (10/20) of cCCCs, including recurrent WWTR1 S89W somatic mutations in 40% (4/10) of the cases harboring mutations in the Hippo pathway. Irrespective of the presence or absence of Hippo pathway genetic alterations, however, all primary cCCCs analyzed in this study (n = 20) harbored features of Hippo pathway deregulation at the transcriptomic and protein levels. In vitro functional analysis revealed that expression of the WWTR1 S89W mutation leads to reduced binding of TAZ to 14-3-3, promoting constitutive nuclear translocation of TAZ and Hippo pathway repression. WWTR1 S89W expression was found to lead to acquisition of oncogenic behavior, including increased proliferation, migration, and colony formation in vitro as well as increased tumorigenesis in vivo, which could be reversed by targeted inhibition of the TAZ/YAP1 complex with verteporfin. Finally, xenografts expressing WWTR1 S89W displayed a shift in tumor phenotype, becoming more infiltrative as well as less differentiated, and were found to be composed of cells with conspicuous cytoplasmic clearing as compared to controls. Our results demonstrate that Hippo pathway alterations are likely drivers of cCCCs and likely contribute to the clear cell phenotype. Therapies targeting this pathway may constitute a new class of treatment for these rare, aggressive tumors. © 2022 The Pathological Society of Great Britain and Ireland.

Details

ISSN :
10969896
Volume :
257
Issue :
5
Database :
OpenAIRE
Journal :
The Journal of pathologyReferences
Accession number :
edsair.doi.dedup.....a4d116d3cc7fa11a12d10028463828e5