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pancreatic ductal adenocarcinoma

Selective Multi-Kinase Inhibition Sensitizes Mesenchymal Pancreatic Cancer to Immune Checkpoint Blockade by Remodeling the Tumor Microenvironment

[Nature Cancer] Scientists performed a systematic high-throughput combination drug screen and identified a synergistic interaction between the MEK inhibitor trametinib and the multi-kinase inhibitor nintedanib, which targeted KRAS-directed oncogenic signaling in mesenchymal PDAC.

Disruption of Pancreatic Stellate Cell Myofibroblast Phenotype Promotes Pancreatic Tumor Invasion

[Cell Reports] Researchers showed that the Rho effector protein kinase N2 (PKN2) was critical for pancreatic stellate cell (PSC) myofibroblast differentiation. Loss of PKN2 was associated with reduced PSC proliferation, contractility, and alpha-smooth muscle actin stress fibers.

Visceral Adipose Tissue Remodeling in Pancreatic Ductal Adenocarcinoma Cachexia: The Role of Activin a Signaling

[Scientific Reports] The authors proposed that activin A signaling could be relevant to the acceleration of visceral adipose tissue wasting in PDAC-associated cachexia.

Karmanos Cancer Institute Awarded $352,000 Grant from U CAN-CER VIVE Foundation

[Karmanos Cancer Institute] The Barbara Ann Karmanos Cancer Institute recently received a $352,437 grant from the U CAN-CER VIVE Foundation to help fund a pancreatic cancer research study.

Panbela Initiates a Randomized, Double-Blind, Placebo-Controlled Study (ASPIRE) of Nab-Paclitaxel and Gemcitabine with or without SBP-101 in Subjects Previously Untreated for Metastatic Pancreatic Ductal...

[Panbela Therapeutics, Inc.] Panbela Therapeutics, Inc. announced the initiation of the company’s global Phase II clinical trial of SBP-101 in combination with Gemcitabine and Nab-Paclitaxel in patients with metastatic pancreatic ductal adenocarcinoma, which is referred to as the ASPIRE trial.

De Novo Expression of Gastrokines in Pancreatic Precursor Lesions Impede the Development of Pancreatic Cancer

[Oncogene] Scientists performed the molecular and histological assessment of patient-derived PanINs, tumor tissues and pancreas from mouse models with PDAC (KC mice that harbor K-RAS mutation in pancreatic tissue), where we noted marked upregulation of gastrokine (GKN) proteins.

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