Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The . gov means it’s official VSports app下载. Federal government websites often end in . gov or . mil. Before sharing sensitive information, make sure you’re on a federal government site. .

Https

The site is secure V体育官网. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. .

. 2007 Aug 15;13(16):4759-68.
doi: 10.1158/1078-0432.CCR-07-0001.

"V体育官网" Targeting neuropilin 1 as an antitumor strategy in lung cancer

Affiliations

Targeting neuropilin 1 as an antitumor strategy in lung cancer

V体育官网 - Tse-Ming Hong et al. Clin Cancer Res. .

Abstract

Purpose: Neuropilin 1 (NRP1) is a mediator of lung branching and angiogenesis in embryonic development and angiogenesis in cancer. The role of NRP1 in cancer progression is not fully elucidated VSports手机版. We investigated the role of NRP1 in cancer invasion and tumor angiogenesis, its signaling pathways, prognostic significance, and therapeutic implications. .

Experimental design: Sixty patients with non-small cell lung cancer (NSCLC) were studied. NRP1 mRNA expression was measured using real-time quantitative reverse-transcription PCR. NRP1 and cancer cell invasion, angiogenesis, and signaling pathways were studied using NRP1 stimulation by vascular endothelial growth factor 165 (VEGF(165)) and NRP1 inhibition by small interfering RNAs (siRNA), soluble NRP1 (sNRP1), and NRP1-inhibition peptides. The NRP1-inhibition peptides were identified using a phage display peptide library V体育安卓版. .

Results: NSCLC patients with high expression of NRP1 had shorter disease-free (P = 0. 0162) and overall survival (P = 0. 0164; log-rank test). Multivariate analyses showed NRP1 is an independent prognostic factor in overall (HR, 2. 37, 95% CI = 1. 15 to 4. 9, P = 0 V体育ios版. 0196) and disease-free survival [hazard ratio (HR), 2. 38; 95% confidence interval (95% CI), 1. 15-4. 91; P = 0. 0195] of NSCLC patients. Knockdown of NRP1 suppressed cancer cell migration, invasion, filopodia formation, tumorigenesis, angiogenesis, and in vivo metastasis. NRP1 signaling pathways involved VEGF receptor 2 and phosphoinositide-3-kinase (PI3K) and Akt activation. Two potent synthetic anti-NRP1 peptides, DG1 and DG2, which block NRP1 signaling pathways and suppress tumorigenesis, cancer invasion, and angiogenesis, were identified. .

Conclusions: NRP1 is a cancer invasion and angiogenesis enhancer. NRP1 expression is an independent predictor of cancer relapse and poor survival in NSCLC patients. NRP1 plays a critical role in tumorigenesis, cancer invasion, and angiogenesis through VEGF, PI3K, and Akt pathways. NRP1 may have potential as a new therapeutic target in NSCLC VSports最新版本. .

PubMed Disclaimer

Publication types

MeSH terms

LinkOut - more resources