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https://doi.org/10.3390/cancers14071652
Title: | PI3K/AKT Signaling Tips the Balance of Cytoskeletal Forces for Cancer Progression | Authors: | Deng, Shuo Leong, Hin Chong Datta, Arpita Gopal, Vennila Kumar, Alan Prem Yap, Celestial T |
Keywords: | Science & Technology Life Sciences & Biomedicine Oncology PI3K AKT cytoskeleton cancer chemotherapy clinical trial PHASE-II TRIAL IXABEPILONE PLUS CAPECITABINE AKT INHIBITOR IPATASERTIB RESISTANT PROSTATE-CANCER ALBUMIN-BOUND PACLITAXEL ANTIBODY-DRUG CONJUGATE BREAST-CANCER INTERMEDIATE-FILAMENTS CELL-MIGRATION PHOSPHOINOSITIDE 3-KINASES |
Issue Date: | 24-Mar-2022 | Publisher: | MDPI | Citation: | Deng, Shuo, Leong, Hin Chong, Datta, Arpita, Gopal, Vennila, Kumar, Alan Prem, Yap, Celestial T (2022-03-24). PI3K/AKT Signaling Tips the Balance of Cytoskeletal Forces for Cancer Progression. CANCERS 14 (7). ScholarBank@NUS Repository. https://doi.org/10.3390/cancers14071652 | Abstract: | The PI3K/AKT signaling pathway plays essential roles in multiple cellular processes, which include cell growth, survival, metabolism, and motility. In response to internal and external stimuli, the PI3K/AKT signaling pathway co-opts other signaling pathways, cellular components, and cytoskeletal proteins to reshape individual cells. The cytoskeletal network comprises three main components, which are namely the microfilaments, microtubules, and intermediate filaments. Collectively, they are essential for many fundamental structures and cellular processes. In cancer, aberrant activation of the PI3K/AKT signaling cascade and alteration of cytoskeletal structures have been observed to be highly prevalent, and eventually contribute to many cancer hallmarks. Due to their critical roles in tumor progression, pharmacological agents targeting PI3K/AKT, along with cytoskeletal components, have been developed for better intervention strategies against cancer. In our review, we first discuss existing evidence in-depth and then build on recent advances to propose new directions for therapeutic intervention. | Source Title: | CANCERS | URI: | https://scholarbank.nus.edu.sg/handle/10635/237212 | ISSN: | 2072-6694 | DOI: | 10.3390/cancers14071652 |
Appears in Collections: | Staff Publications Elements |
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