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Targeting apoptotic pathways for cancer therapy.
Tian, Xiaobing; Srinivasan, Praveen R; Tajiknia, Vida; Sanchez Sevilla Uruchurtu, Ashley F; Seyhan, Attila A; Carneiro, Benedito A; De La Cruz, Arielle; Pinho-Schwermann, Maximilian; George, Andrew; Zhao, Shuai; Strandberg, Jillian; Di Cristofano, Francesca; Zhang, Shengliang; Zhou, Lanlan; Raufi, Alexander G; Navaraj, Arunasalam; Zhang, Yiqun; Verovkina, Nataliia; Ghandali, Maryam; Ryspayeva, Dinara; El-Deiry, Wafik S.
Afiliación
  • Tian X; Laboratory of Translational Oncology and Experimental Cancer Therapeutics and.
  • Srinivasan PR; Department of Pathology and Laboratory Medicine, Warren Alpert Medical School, Brown University, Providence, Rhode Island, USA.
  • Tajiknia V; Joint Program in Cancer Biology, Lifespan Health System and Brown University, Providence, Rhode Island, USA.
  • Sanchez Sevilla Uruchurtu AF; Legorreta Cancer Center at Brown University, Providence, Rhode Island, USA.
  • Seyhan AA; Laboratory of Translational Oncology and Experimental Cancer Therapeutics and.
  • Carneiro BA; Department of Pathology and Laboratory Medicine, Warren Alpert Medical School, Brown University, Providence, Rhode Island, USA.
  • De La Cruz A; Joint Program in Cancer Biology, Lifespan Health System and Brown University, Providence, Rhode Island, USA.
  • Pinho-Schwermann M; Legorreta Cancer Center at Brown University, Providence, Rhode Island, USA.
  • George A; Laboratory of Translational Oncology and Experimental Cancer Therapeutics and.
  • Zhao S; Department of Pathology and Laboratory Medicine, Warren Alpert Medical School, Brown University, Providence, Rhode Island, USA.
  • Strandberg J; Joint Program in Cancer Biology, Lifespan Health System and Brown University, Providence, Rhode Island, USA.
  • Di Cristofano F; Legorreta Cancer Center at Brown University, Providence, Rhode Island, USA.
  • Zhang S; Laboratory of Translational Oncology and Experimental Cancer Therapeutics and.
  • Zhou L; Department of Pathology and Laboratory Medicine, Warren Alpert Medical School, Brown University, Providence, Rhode Island, USA.
  • Raufi AG; Joint Program in Cancer Biology, Lifespan Health System and Brown University, Providence, Rhode Island, USA.
  • Navaraj A; Legorreta Cancer Center at Brown University, Providence, Rhode Island, USA.
  • Zhang Y; Pathobiology Graduate Program, Brown University, Providence, Rhode Island, USA.
  • Verovkina N; Laboratory of Translational Oncology and Experimental Cancer Therapeutics and.
  • Ghandali M; Department of Pathology and Laboratory Medicine, Warren Alpert Medical School, Brown University, Providence, Rhode Island, USA.
  • Ryspayeva D; Joint Program in Cancer Biology, Lifespan Health System and Brown University, Providence, Rhode Island, USA.
  • El-Deiry WS; Legorreta Cancer Center at Brown University, Providence, Rhode Island, USA.
J Clin Invest ; 134(14)2024 Jul 15.
Article en En | MEDLINE | ID: mdl-39007268
ABSTRACT
Apoptosis is a form of programmed cell death that is mediated by intrinsic and extrinsic pathways. Dysregulation of and resistance to cell death are hallmarks of cancer. For over three decades, the development of therapies to promote treatment of cancer by inducing various cell death modalities, including apoptosis, has been a main goal of clinical oncology. Apoptosis pathways also interact with other signaling mechanisms, such as the p53 signaling pathway and the integrated stress response (ISR) pathway. In addition to agents directly targeting the intrinsic and extrinsic pathway components, anticancer drugs that target the p53 and ISR signaling pathways are actively being developed. In this Review, we discuss selected and promising anticancer therapies in various stages of development, including drug targets, mechanisms, and resistance to related treatments, focusing especially on B cell lymphoma 2 (BCL-2) inhibitors, TRAIL analogues, DR5 antibodies, and strategies that target p53, mutant p53, and the ISR.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transducción de Señal / Proteína p53 Supresora de Tumor / Apoptosis / Neoplasias Límite: Animals / Humans Idioma: En Revista: J Clin Invest Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transducción de Señal / Proteína p53 Supresora de Tumor / Apoptosis / Neoplasias Límite: Animals / Humans Idioma: En Revista: J Clin Invest Año: 2024 Tipo del documento: Article
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