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NSCLC

DLX6-AS1 Activated by H3K4me1 Enhanced Secondary Cisplatin Resistance of Lung Squamous Cell Carcinoma through Modulating miR-181a-5p/miR-382-5p/CELF1 Axis

[Scientific Reports] Secondary cisplatin resistance majorly undermines the cisplatin efficacy leading to a worse prognosis. In this respect, researchers identified the role of the DLX6-AS1/miR-181a-5p/miR-382-5p/CELF1 axis in regulating cisplatin resistance of lung squamous cell carcinoma.

GOLPH3/CKAP4 Promotes Metastasis and Tumorigenicity by Enhancing the Secretion of Exosomal WNT3A in Non-Small-Cell Lung Cancer

[Cell Death & Disease] Scientists evaluated the function of golgi phosphoprotein 3 (GOLPH3) in non-small-cell lung cancer (NSCLC) distal metastasis. GOLPH3 was expressed at high levels in samples from patients with NSCLC and was positively associated with clinicopathologic characteristics including clinical stage classification.

Dysregulation of TFH-B-TRM Lymphocyte Cooperation Is Associated with Unfavorable Anti-PD-1 Responses in EGFR-Mutant Lung Cancer

[Nature Communications] Hypothesizing that EGFR mutations alter tumor-immune interactions, scientists compared tumor-infiltrating lymphocytes between EGFR mutant and wild type tumors through single-cell transcriptomic analysis.

Treating Disease Progression with Osimertinib in EGFR-Mutated Non-Small Cell Lung Cancer: Novel Targeted Agents and Combination Strategies

[ESMO Open] In this review, the post-osimertinib treatment options for EGFR-mutated non-small-cell lung cancer are analyzed, with an outlook to ongoing clinical trials.

An SETD1A/Wnt/β-Catenin Feedback Loop Promotes NSCLC Development

[Journal of Experimental & Clinical Cancer Research] Researchers found that SETD1A positively regulated the Wnt/β-catenin pathway via interacting with and stabilizing β-catenin.

Potentiated Lung Adenocarcinoma (LUAD) Cell Growth, Migration and Invasion by lncRNA DARS-AS1 via miR-188-5p/ KLF12 Axis

[Aging] Cell functional experiments revealed that lncRNA DARS-AS1 participated in enhancing lung adenocarcinoma proliferation, invasion, and migration by inhibiting miR-188-5p.

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