 | Vol. 11.16 – 28 April, 2022 |
| |
|
|
| Scientists suggested that a stimuli-responsive dendritic polymer-based nano-cocktail therapy may provide a promising approach for the treatment of epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) resistant NSCLC. [Advanced Materials] |
|  |
|
|
PUBLICATIONSRanked by the impact factor of the journal |
|
|
|
| Researchers showed that SARS-CoV-2 readily infected and replicated in human-induced pluripotent stem cell-derived proximal airway cells, distal alveolar cells, and lung progenitors. [Journal of Cellular Physiology] |
|
|
|
| The authors investigated the therapeutic potential of HOTAIRM1 transferred by alveolar epithelial cell-derived exosomes in interstitial pulmonary fibrosis and the potential molecular mechanisms. [Laboratory Investigation] |
| |
|
|
| Investigators demonstrated that a loss-of-function mutation of the major histone lysine methyltransferase SETDB1 possessing oncogenic activity in lung cancer cells led to broad changes in the overall architecture and mechanical properties of the nucleus through genome. [Nucleic Acids Research] |
|
|
|
| Kelch domain containing 3 (KLHDC3) shortage significantly increased the sensitivity of lung cancer cells to epidermal growth factor receptor-targeted drugs, providing an alternative explanation for the development of Gefitinib and Osimertinib resistance in NSCLC therapy. [Oncogene] |
|
|
|
| High-throughput RNA sequencing was performed to identify significantly expressed circular RNAs in NSCLC tissues. The functions of circ-0001875 in NSCLC cells were investigated in vitro and in vivo. [Journal of Experimental & Clinical Cancer Research] |
|
|
|
| Scientists reported that the expression of SHANK1 was upregulated in NSCLC, and was correlated with clinic pathological characteristics of NSCLC. [Cell Death & Disease] |
|
|
|
| Researchers found that tongue cancer resistance-associated protein (TCRP1) was increased in p53-mutant NSCLC, comparing to that in NSCLC with wild type p53. [Oncogenesis] |
|
|
|
| The efficacy of chloroquine in combination with lorlatinib in anaplastic lymphoma kinase-positive NSCLC cells in vitro and in vivo was assessed using CCK-8, colony formation, immunofluorescence staining, flow cytometry analysis, western blot analysis, and xenograft implantation. [Cell Death Discovery] |
|
|
|
| Targeting Hsa-miR-22-3p and Hsa-miR-184 desensitized EGFR-mutated NSCLC cells to Osimertinib. [Scientific Reports] |
|
|
|
| Researchers suggested that integrin αvβ3 could efficiently promote lung cancer cell proliferation and stem-like phenotypes in a tribbles homolog 3 (TRIB3) dependent manner. [BMC Cancer] |
|
|
|
| Circ_0072088-dependent regulation of miR-1261/PIK3CA was important for cell proliferation, migration, and invasion during the tumorigenesis and progression of lung adenocarcinoma. [Thoracic Cancer] |
|
|
|
|
| The authors discuss regulation of lncRNAs by anti-cancer drugs and genetic tools as well as the role of these factors in therapy response of lung cancer cells. [Biomedicine & Pharmacotherapy] |
|
|
|
| Scientists deliver up-to-date research in nanostructured therapies in inflammatory lung diseases with an emphasis on biocomposite-based nanoparticles. [Nanomedicine] |
|
|
|
|
| ImmunityBio, Inc. announced that the first participants have been enrolled in a study that is part of an 800-site master protocol trial for NSCLC. The Lung Cancer Master Protocol trial (Lung-MAP) includes a study of Anktivaâ„¢ plus Keytruda versus investigator choice of standard-of-care chemotherapy in patients with NSCLC. [ImmunityBio, Inc.] |
|
|
|
| Novartis announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency adopted a positive opinion and recommended granting marketing authorization of Tabrecta® as a monotherapy for the treatment of adults with advanced NSCLC. [Novartis] |
|
|
|
| OncoC4, Inc. announced that the US FDA has granted Fast Track designation to ONC-392, the company’s next-gen anti-CTLA-4 monoclonal antibody as a single agent for the treatment of patients with metastatic non-small cell lung carcinoma (NSCLC) who have had disease progression on prior anti-PD-(L)1 therapy. [OncoC4, Inc.] |
|
|
|
|
| September 7 – 11, 2022 Woods Hole, Massachusetts, United States |
|
|
|
|
|
| Mayo Clinic – Scottsdale, Arizona, United States |
|
|
|
| Gilead Sciences, Inc. – Foster City, California, United States |
|
|
|
| McGill University – Montreal, Quebec, Canada |
|
|
|
| Medical Center Cologne – Cologne, Germany |
|
|
|
| The Ohio State University – Columbus, Ohio, United States |
|
|
|
|