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Prognostic role of TEAD4 in TNBC: in-silico inhibition of the TEAD4-YAP interaction by flufenamic acid analogs.
Gupta, Shradheya R R; Singh, Shivani; Rustagi, Vanshika; Pahuja, Monika; Mangangcha, Irengbam Rocky; Rinchui, Moses; Jha, Saurabh K; Singh, Archana; Singh, Indrakant K.
Afiliación
  • Gupta SRR; Molecular Biology Research Laboratory, Department of Zoology, & DBC I4 Centre, Deshbandhu College, University of Delhi, New Delhi, 110019 India.
  • Singh S; Molecular Biology Research Laboratory, Department of Zoology, & DBC I4 Centre, Deshbandhu College, University of Delhi, New Delhi, 110019 India.
  • Rustagi V; Department of Biotechnology, Sharda School of Engineering and Technology, Sharda University, Greater Noida, 201310 India.
  • Pahuja M; Molecular Biology Research Laboratory, Department of Zoology, & DBC I4 Centre, Deshbandhu College, University of Delhi, New Delhi, 110019 India.
  • Mangangcha IR; Extramural Wing, Indian Council of Medical Research, New Delhi, 110029 India.
  • Rinchui M; Molecular Biology Research Laboratory, Department of Zoology, & DBC I4 Centre, Deshbandhu College, University of Delhi, New Delhi, 110019 India.
  • Jha SK; Molecular Biology Research Laboratory, Department of Zoology, & DBC I4 Centre, Deshbandhu College, University of Delhi, New Delhi, 110019 India.
  • Singh A; Department of Zoology, Kalindi College, University of Delhi, New Delhi, 110008 India.
  • Singh IK; Department of Plant Molecular Biology, University of Delhi South Campus, Benito Juarez Marg, New Delhi, 110021 India.
In Silico Pharmacol ; 12(2): 64, 2024.
Article en En | MEDLINE | ID: mdl-39035099
ABSTRACT
Triple-negative breast cancer (TNBC) poses a significant global health challenge due to its highly aggressive nature and invasive characteristics. Dysregulation of the Hippo pathway, a key regulator of various biological processes, is observed in TNBC, and its inhibition holds promise for impeding cancer growth. This in-silico analysis investigates the role of Transcriptional Enhanced Associate Domain 4 (TEAD4) in TNBC and its interaction with Yes Associated Protein (YAP) in cancer progression. Our results demonstrate that TEAD4 upregulation is linked to poor prognosis in TNBC, emphasizing its critical role in the disease. Moreover, we identify CID44521006, an analog of Flufenamic acid, as a potential therapeutic compound capable of disrupting the TEAD4-YAP interaction by binding to the YAP-binding domain of TEAD4. These findings underscore the significance of TEAD4 in TNBC and propose CID44521006 as a promising candidate for therapeutic intervention. The study contributes valuable insights to advance treatment options for TNBC, offering a potential avenue for the development of targeted therapies against this aggressive form of breast cancer. Supplementary Information The online version contains supplementary material available at 10.1007/s40203-024-00239-8.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: In Silico Pharmacol Año: 2024 Tipo del documento: Article Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: In Silico Pharmacol Año: 2024 Tipo del documento: Article Pais de publicación: Alemania