TY - JOUR
T1 - Janus Kinase–Signal Transducer and Activator of Transcription Inhibitors for the Treatment and Management of Cancer
AU - Rizwi, Fahim Anwar
AU - Abubakar, Md
AU - Puppala, Eswara Rao
AU - Goyal, Ahsas
AU - Bhadrawamy, Ch Veera
AU - Naidu, V. G.M.
AU - Roshan, S.
AU - Tazneem, B.
AU - Almalki, Waleed Hassan
AU - Subramaniyan, Vetriselvan
AU - Rawat, Sushama
AU - Guptah, Gaurav
N1 - Publisher Copyright:
© 2023 by Begell House, Inc.
PY - 2023
Y1 - 2023
N2 - According to the World Health Organization (WHO), cancer is the second-highest cause of mortality worldwide, killing nearly 9.6 million people annually. Despite the advances in diagnosis and treatment during the last couple of decades, it remains a serious concern due to the limitations of currently available cancer management strategies. Therefore, alternative strategies are highly required to overcome these glitches. In addition, many etiological factors such as environmental and genetic factors initiate the activation of the Janus kinase (JAK)–signal transducer and activator of the transcription (STAT) pathway. This aberrant activation of the JAK–STAT pathway has been reported in various disease states, including inflammatory conditions, hematologic malignancies, and cancer. For instance, many patients with myeloproliferative neoplasms carry the acquired gain-of-function JAK2 V617F somatic mutation. This knowledge has dramatically improved our understanding of pathogenesis and has facilitated the development of therapeutics capable of suppressing the constitutive activation of the JAK–STAT pathway. Our aim is not to be expansive but to highlight emerging ideas towards preventive therapy in a modern view of JAK–STAT inhibitors. A series of agents with different specificities against different members of the JAK family of proteins is currently undergoing evaluation in clinical trials. Here we give a summary of how JAK–STAT inhibitors function and a detailed review of current clinical drugs for managing cancer as a new therapeutic approach.
AB - According to the World Health Organization (WHO), cancer is the second-highest cause of mortality worldwide, killing nearly 9.6 million people annually. Despite the advances in diagnosis and treatment during the last couple of decades, it remains a serious concern due to the limitations of currently available cancer management strategies. Therefore, alternative strategies are highly required to overcome these glitches. In addition, many etiological factors such as environmental and genetic factors initiate the activation of the Janus kinase (JAK)–signal transducer and activator of the transcription (STAT) pathway. This aberrant activation of the JAK–STAT pathway has been reported in various disease states, including inflammatory conditions, hematologic malignancies, and cancer. For instance, many patients with myeloproliferative neoplasms carry the acquired gain-of-function JAK2 V617F somatic mutation. This knowledge has dramatically improved our understanding of pathogenesis and has facilitated the development of therapeutics capable of suppressing the constitutive activation of the JAK–STAT pathway. Our aim is not to be expansive but to highlight emerging ideas towards preventive therapy in a modern view of JAK–STAT inhibitors. A series of agents with different specificities against different members of the JAK family of proteins is currently undergoing evaluation in clinical trials. Here we give a summary of how JAK–STAT inhibitors function and a detailed review of current clinical drugs for managing cancer as a new therapeutic approach.
KW - cancer
KW - clinical drugs
KW - JAK–STAT pathway
KW - treatment
KW - tyrosine kinase
UR - http://www.scopus.com/inward/record.url?scp=85169173451&partnerID=8YFLogxK
U2 - 10.1615/JEnvironPatholToxicolOncol.2023045403
DO - 10.1615/JEnvironPatholToxicolOncol.2023045403
M3 - Article
C2 - 37522565
AN - SCOPUS:85169173451
SN - 0731-8898
VL - 42
SP - 15
EP - 29
JO - Journal of Environmental Pathology, Toxicology and Oncology
JF - Journal of Environmental Pathology, Toxicology and Oncology
IS - 4
ER -