AI Article Synopsis

  • G protein-coupled receptors (GPCRs), especially GPR171, play a significant role in lung cancer growth and metastasis, with GPR171 found to be overexpressed in about 46.8% of lung carcinoma samples.
  • Depleting GPR171 using an anti-GPR171 antibody reduces lung cancer cell proliferation and slows tumor progression in mice, while knocking down GPR171 inhibits cancer cell migration and invasion.
  • Targeting GPR171 shows promise as a cancer treatment strategy, especially when combined with epidermal growth factor receptor (EGFR) inhibitors to enhance their effectiveness.

Article Abstract

G protein-coupled receptors (GPCRs) are among the most significant therapeutic targets and some of them promote the growth and metastasis of cancer. Here, we show that an increase in the levels of GPR171 is crucial for lung cancer tumor progression in vitro and in vivo. Immunostaining of clinical samples indicated that GPR171 was overexpressed in 46.8% of lung carcinoma tissues. Depletion of GPR171 with an anti-GPR171 antibody decreased proliferation of lung carcinoma cells and attenuated tumor progression in a mouse xenograft model. Knockdown of GPR171 also inhibited migration and invasion of the lung cancer cell lines. Notably, inhibition of GPR171 synergistically enhanced the tumoricidal activity of an epidermal growth factor receptor (EGFR) inhibitor in lung cancer cells. These results indicate that GPR171 blockade is a promising antineoplastic strategy and provide a preclinical rationale for combined inhibition of GPR171 and EGFR.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884959PMC
http://dx.doi.org/10.18632/oncotarget.6856DOI Listing

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