- |||||||||| Halaven (eribulin mesylate) / Eisai, Aliqopa (copanlisib) / Bayer
Enrollment closed, Combination therapy, Metastases: Testing the Addition of Copanlisib to Eribulin for the Treatment of Advanced-Stage Triple Negative Breast Cancer (clinicaltrials.gov) - Nov 29, 2023 P1/2, N=106, Active, not recruiting, Together, the browning of mammary fat suppressed the development of the pubertal mammary gland, which was associated with the elevated serum DOPC and the inhibition of the PI3K/Akt pathway. Suspended --> Active, not recruiting
- |||||||||| sirolimus / Generic mfg.
Journal: Curcumin inhibits the activity and induces apoptosis of activated hepatic stellate cell by suppressing autophagy. (Pubmed Central) - Nov 27, 2023 Our results showed that rapamycin, an autophagy activator, could partly offset the effects of curcumin on autophagy and apoptosis of LX-2 cells, while 3-Methyladenine (3-MA), an autophagy inhibitor, could enhance these effects...Overall, we demonstrated that curcumin could inhibit the activity and promote LX-2 cells apoptosis by suppressing autophagy by activating the PI3K/Akt/mTOR signal pathway. In addition, lipid recovery and energy deprivation due to autophagy inhibition may be the exact mechanism by which curcumin attenuates the pro-fibrotic activity of LX-2.
- |||||||||| Journal, PD(L)-1 Biomarker, IO biomarker: BATF2 inhibits PD-L1 expression and regulates CD8T cells infiltration in non-small cell lung cancer. (Pubmed Central) - Nov 27, 2023
Based on bioinformatics analysis, we found the function of BATF2 in promoting anti-tumor immune response in patients with NSCLC, which is mediated by BATF2 enhances CD8 T cells infiltration as well as activation. BATF2 from circulating and tissue can serve as an efficient biomarker to predict diagnosis, prognosis and immunotherapy efficacy.
- |||||||||| Journal: Protein interaction network analysis of mTOR signaling reveals modular organization. (Pubmed Central) - Nov 27, 2023
Using primary fibroblasts from individuals with overgrowth disorders caused by pathogenic PIK3CA or MTOR variants, we find that hyperactivation of mTOR pathway components is reflected in a hyperactive PIN. Our data define a "modular" organization of the mTOR PIN in which coordinated groups of interactions respond to activation or inhibition of distinct nodes, and demonstrate that kinase inhibitors affect the modular network architecture in a complex manner, inconsistent with simple linear models of signal transduction.
- |||||||||| Journal, Myeloid-derived suppressor cells: Myeloid-derived suppressor cells and tolerogenic dendritic cells are distinctively induced by PI3K and Wnt signaling pathways. (Pubmed Central) - Nov 27, 2023
The identification of PI3K-AKT and Wnt signal transduction pathways as respective inducers of the immunomodulatory capacity of M-MDSCs and TolDCs provides opportunities to overcome suppressive myeloid cells in cancer patients and optimize therapeutic application of TolDCs in patients with autoimmune diseases. Lastly, the observed similarities between generated- and patient-derived M-MDSCs support the use of in vitro generated M-MDSCs as powerful model to investigate the functionality of human MDSCs.
- |||||||||| Journal: Rational Combinations of PARP Inhibitors with HRD-Inducing Molecularly Targeted Agents. (Pubmed Central) - Nov 22, 2023
Cancers with wild-type BRCA, homologous recombination proficiency, or de novo or acquired resistance to PARP inhibition represent a growing population of patients who may benefit from combinatorial PARP inhibitor strategies. We review targeted inhibitors of angiogenesis, epigenetic regulators, and PI3K, MAPK, and other cellular signaling pathways as inducers of homologous recombination deficiency, providing support for the use of PARP inhibitors in contexts not previously considered susceptible to PARP inhibition.
- |||||||||| LY294002 / Eli Lilly
Journal: Nodakenin alleviates ovariectomy-induced osteoporosis by modulating osteoblastogenesis and osteoclastogenesis. (Pubmed Central) - Nov 22, 2023 In contrast, LY294002, an inhibitor of PI3K, reversed these changes and inhibited the osteogenic differentiation-enabling effect of NK...In addition, oral administration of NK to mice significantly elevated bone mass and ameliorated ovariectomized (OVX)-mediated bone microarchitectural disorders. In conclusion, these data suggest that NK attenuates OVX-induced bone loss by enhancing osteogenesis and inhibiting osteoclastogenesis.
- |||||||||| Halaven (eribulin mesylate) / Eisai, Aliqopa (copanlisib) / Bayer
Trial suspension, Combination therapy, Metastases: Testing the Addition of Copanlisib to Eribulin for the Treatment of Advanced-Stage Triple Negative Breast Cancer (clinicaltrials.gov) - Nov 22, 2023 P1/2, N=106, Suspended, ISOX, apicidin, and panobinostat were promising similar drugs and that GSK-1059615, alisertib, and avrainvillamide-analog-6 were promising ancillary drugs to TSA in the treatment of DE. Recruiting --> Suspended
- |||||||||| LY294002 / Eli Lilly
Journal: Hyperoside Prevents A?42-Induced Neurotoxicity in PC12 Cells and Caenorhabditis elegans. (Pubmed Central) - Nov 21, 2023 The results of molecular docking further indicated that the PI3K/Akt pathways may be involved in the protection of A?42-induced PC12 cells by hyperoside treatment. The study provides theoretical information for research and development of hyperoside as an antioxidant dietary supplement.
- |||||||||| Ukoniq (umbralisib) / TG Therap, Briumvi (ublituximab-xiiy) / TG Therap, Neuraxpharm, Calquence (acalabrutinib) / AstraZeneca
Trial completion date, Combination therapy: Acalabrutinib, Umbralisib, and Ublituximab for the Treatment of Previously Untreated Mantle Cell Lymphoma (clinicaltrials.gov) - Nov 18, 2023 P2, N=12, Active, not recruiting, and cfDNA, in adipocytic CAMP expression as a novel putative molecular mechanism in adipose tissue innate immunity. Trial completion date: Sep 2023 --> Sep 2025
- |||||||||| Review, Journal: PI3K/Akt/mTOR Signaling Pathway in Blood Malignancies-New Therapeutic Possibilities. (Pubmed Central) - Nov 14, 2023
Recently, new inhibitors of PI3K/Akt/mTOR signaling have been developed and tested both in preclinical and clinical models. In this review, we outline the role of the PI3K/Akt/mTOR signaling pathway in blood malignancies' cells and gather information on the inhibitors of this pathway that might provide a novel therapeutic opportunity against leukemia.
- |||||||||| Xalkori (crizotinib) / Pfizer, Votrient (pazopanib) / Novartis, BeiGene
Review, Journal: Antiangiogenics in Malignant Granular Cell Tumors: Review of the Literature. (Pubmed Central) - Nov 14, 2023 Dasatinib and megestrol were ineffective in two other different patients. Pazopanib has been demonstrated to be active in advanced GCTs and may be considered as a preferable treatment option.
- |||||||||| LY294002 / Eli Lilly
Journal: Tongqiao Mingmu formula alleviates retinal ganglion cell autophagy through PI3K/AKT/mTOR pathway. (Pubmed Central) - Nov 14, 2023 However, TQMM formula serum could generate an opposite effect and upregulate the expressions of the PI3K/AKT/mTOR pathway genes and proteins. In conclusion, the TQMM formula can prevent glutamate-induced autophagy in RGCs, possibly by activating the PI3K/AKT/mTOR pathway and reducing the expression of autophagy-related biomarkers LC3 and Belicin-1 to attenuate autophagy and maintain RGC viability.
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