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PI3K

Novel Inhibitor of Hematopoietic Cell Kinase as a Potential Therapeutic Agent for Acute Myeloid Leukemia

[Cancer Immunology Immunotherapy] Scientists investigated in vitro, ex vivo and in vivo effects of a novel chemical compound targeting HCK inhibition, in combination with the most used drugs for the treatment of myelodysplastic syndrome and de novo acute myeloid leukemia, 5-Azacytidine and Cytarabine.

Focal Adhesion Kinase Plays a Dual Role in TRAIL Resistance and Metastatic Outgrowth of Malignant Melanoma

[Cell Death & Disease] The authors showed 2nd generation hexameric TRAIL-receptor-agonist IZI1551 to effectively induce apoptosis in malignant melanoma cells irrespective of the intrinsic BRAF/NRAS mutation status.

Cathelicidin hCAP18/LL-37 Promotes Cell Proliferation and Suppresses Antitumor Activity of 1,25(OH)2D3 in Hepatocellular Carcinoma

[Cell Death Discovery] Scientists investigated the effects of hCAP18/LL-37 on hepatocellular carcinoma (HCC) in vitro and in vivo. Results showed that hCAP18/LL-37 overexpression significantly promoted the proliferation of cultured HCC cells and the growth of PLC/PRF-5 xenograft tumor.

Overcoming Resistance to Immune Checkpoint Therapy in PTEN-Null Prostate Cancer by Intermittent Anti-PI3Kα/β/δ Treatment

[Nature Communications] Scientists found that intermittent but not daily dosing of a PI3Kα/β/δ inhibitor, BAY1082439, on Pten-null prostate cancer models could overcome immune checkpoint therapy resistance and unleash CD8+ T cell-dependent anti-tumor immunity in vivo.

VLCAD Inhibits the Proliferation and Invasion of Hepatocellular Cancer Cells through Regulating PI3K/AKT Axis

[Clinical and Translational Oncology] Researchers aimed to investigate the role and underlying molecule mechanism of very-long-chain acyl-CoA dehydrogenase (VLCAD) in the pathological process of hepatocellular carcinoma.

MAPK4 Promotes Triple Negative Breast Cancer Growth and Reduces Tumor Sensitivity to PI3K Blockade

[Nature Communications] Researchers demonstrated that a large subset of TNBC expressed significant levels of MAPK4, and this expression was critical for driving AKT activation independent of PI3K and promoting TNBC cell and xenograft growth.

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