PI3K inhib 
Welcome,         Profile    Billing    Logout  
 67 Companies  59 Products   59 Products   344 Diseases   342 Trials   12240 News 


«12...2122232425262728293031...229230»
  • ||||||||||  ethambutol / Generic mfg.
    Journal:  Protease-Activated Receptor-2 and Phospholipid Metabolism Analysis in Hyperuricemia-Induced Renal Injury. (Pubmed Central) -  Jul 28, 2023   
    We induced a hyperuricemia model in rats by adenine and ethambutol gavage in an in vivo experiment...Our work suggests that PAR2 may mediate hyperuricemia-mediated renal injury by activating the PI3K/AKT/NF-?B pathway. The PAR2 antagonist AZ3451 may be a promising therapeutic strategy for hyperuricemia-induced inflammatory responses.
  • ||||||||||  parsaclisib (INCB50465) / Incyte
    Trial completion date:  CITADEL-203: A Study of INCB050465 in Relapsed or Refractory Follicular Lymphoma (clinicaltrials.gov) -  Jul 28, 2023   
    P2,  N=126, Active, not recruiting, 
    The PAR2 antagonist AZ3451 may be a promising therapeutic strategy for hyperuricemia-induced inflammatory responses. Trial completion date: Jun 2023 --> Jul 2024
  • ||||||||||  LY294002 / Eli Lilly
    Journal:  Secreted phosphoprotein 1 exacerbates renal ischemia-reperfusion injury by inhibiting PI3K/AKT signaling pathway. (Pubmed Central) -  Jul 28, 2023   
    In vitro and in vivo studies revealed an increase in cell apoptosis due to SPP1 overexpression, but the opposite is true when SPP1 is silenced. SPP1 downregulation led to high p-PI3K and p-AKT protein levels, and the LY294002 application inhibited SPP1 inhibition-mediated anti-apoptotic effect Taken together, SPP1 exacerbates renal IRI in vivo and in vitro via promoting programmed cell death by inhibiting PI3K/AKT signaling pathway.
  • ||||||||||  Preclinical, Journal:  Efficacy of combined targeted therapy with PI3K and CDK4/6 or PARP and WEE1 inhibitors in neuroblastoma cell lines. (Pubmed Central) -  Jul 25, 2023   
    Moreover, combining MK?1775 and BMN673 decreased the numbers of cells in S phase to a greater extent than either drug alone, while when combining PD?0332991 and BYL719 the observed effect was close to that of PD?0332991 alone. To summarize, PI3K and CDK4/6 or PARP and WEE1 exhibited synergistic anti?NB effects and lower doses of the inhibitors could be utilized, thereby potentially reducing adverse side effects.
  • ||||||||||  SOX2 Deregulated Squamous Carcinomas Are Vulnerable to AKT3 Inhibition (Exhibit Hall) -  Jul 25, 2023 - Abstract #IASLCWCLC2023IASLC_WCLC_1212;    
    The PI3K/AKT signaling pathway is involved in reduced sensitivity of cancer cells to TTFields treatment, and PI3K inhibition may allow sensitization to TTFields. Taken together, our work suggests that SOX2-amplified squamous cancers may be vulnerable to isoform-specific inhibition of AKT3.
  • ||||||||||  Retrospective data, Review, Journal, Metastases, Discordant:  Discordance of PIK3CA mutational status between primary and metastatic breast cancer: a systematic review and meta-analysis. (Pubmed Central) -  Jul 24, 2023   
    Targeting the PI3K/Akt pathway has tremendous potential as a therapeutic strategy for regulating macrophage polarization and activity to treat chronic liver diseases with plant chemicals, providing new avenues for liver disease treatment. Our results indicate the need of obtaining metastatic biopsies for PIK3CA-mutation analysis and the possibility of testing of the primary tumor, in case a re-biopsy deemed non-feasible.
  • ||||||||||  parsaclisib (INCB50465) / Incyte
    Trial completion date, Trial primary completion date:  Open-Label Study of Parsaclisib, in Japanese Participants With Relapsed or Refractory Follicular Lymphoma (CITADEL-213) (clinicaltrials.gov) -  Jul 20, 2023   
    P2,  N=42, Active, not recruiting, 
    These results showed that the QZJT can enhance podocyte autophagy and ameliorate podocyte injury in DKD by inhibiting the PI3K/AKT/mTOR signaling pathway. Trial completion date: Feb 2024 --> Oct 2023 | Trial primary completion date: Feb 2024 --> Feb 2023
  • ||||||||||  Journal:  The mechanisms of class 1A PI3K and Wnt/?-catenin coupled signaling in breast cancer. (Pubmed Central) -  Jul 20, 2023   
    However, PI3K exhibits opposing effects on Wnt/?-catenin signaling in distinct tumor subsets, whereby PI3K promotes Wnt/?-catenin activation in ER+ cancers, but paradoxically suppresses this pathway in ER- breast cancers. This review discusses the molecular mechanisms for PI3K-Wnt crosstalk in breast cancer, and how Wnt-targeted therapies have the potential to contribute to treatment regimens for breast cancers with PI3K dysregulation.
  • ||||||||||  Journal:  1-Methoxyerythrabyssin II Induces Autophagy in Leukemia Cells via PI3K/Akt/mTOR Pathways. (Pubmed Central) -  Jul 17, 2023   
    In vitro assays further demonstrated that 1-methoxyerythrabyssin II promoted autophagy and suppressed cell proliferation by inhibiting the PI3K/Akt/mTOR pathway in leukemic cells. This discovery will contribute to the development of novel therapeutics and prophylactics against leukemia.
  • ||||||||||  SL-901 / Menarini
    Trial completion, Enrollment change, Trial completion date, Trial primary completion date, Metastases:  Study of the PI3K Inhibitor SL-901 in Patients With Advanced Solid Tumors With Advanced Solid Tumors (clinicaltrials.gov) -  Jul 12, 2023   
    P1,  N=20, Completed, 
    Recruiting --> Active, not recruiting Recruiting --> Completed | N=60 --> 20 | Trial completion date: Dec 2023 --> Jun 2023 | Trial primary completion date: Dec 2023 --> May 2023