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Recurrent WWTR1 S89W mutations and Hippo pathway deregulation in clear cell carcinomas of the cervix.
Kim, Sarah H; Basili, Thais; Dopeso, Higinio; Da Cruz Paula, Arnaud; Bi, Rui; Issa Bhaloo, Shirin; Pareja, Fresia; Li, Qing; da Silva, Edaise M; Zhu, Yingjie; Hoang, Timothy; Selenica, Pier; Murali, Rajmohan; Chan, Eric; Wu, Michelle; Derakhshan, Fatemeh; Maroldi, Ana; Hanlon, Etta; Ferreira, Carlos Gil; Lapa E Silva, Jose Roberto; Abu-Rustum, Nadeem R; Zamarin, Dmitriy; Chandarlapaty, Sarat; Matrai, Cathleen; Yoon, Ju-Yoon; Reis-Filho, Jorge S; Park, Kay J; Weigelt, Britta.
Affiliation
  • Kim SH; Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Basili T; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Dopeso H; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Da Cruz Paula A; Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Bi R; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Issa Bhaloo S; Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, PR China.
  • Pareja F; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Li Q; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • da Silva EM; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Zhu Y; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Hoang T; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Selenica P; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Murali R; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Chan E; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Wu M; Molecular Cytology Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Derakhshan F; Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Maroldi A; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Hanlon E; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Ferreira CG; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Lapa E Silva JR; Oncoclinicas Institute for Research and Education, Sao Paulo, Brazil.
  • Abu-Rustum NR; Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Zamarin D; Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Chandarlapaty S; Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Matrai C; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Yoon JY; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Reis-Filho JS; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Park KJ; Department of Pathology, Weill Cornell Medical Center, New York, NY, USA.
  • Weigelt B; Department of Pathology, St Michael's Hospital, Unity Health Toronto, Toronto, Canada.
J Pathol ; 257(5): 635-649, 2022 08.
Article in En | MEDLINE | ID: mdl-35411948
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Trans-Activators / Hippo Signaling Pathway Type of study: Prognostic_studies Limits: Female / Humans Language: En Journal: J Pathol Year: 2022 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Trans-Activators / Hippo Signaling Pathway Type of study: Prognostic_studies Limits: Female / Humans Language: En Journal: J Pathol Year: 2022 Document type: Article Affiliation country: United States Country of publication: United kingdom