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Down-regulated NEDD4L facilitates tumor progression through activating Notch signaling in lung adenocarcinoma
Liping Lin1,2, Xuan Wu3, Yuanxue Jiang1,2
1Department of Oncology, Panyu Central Hospital, Guangzhou, Guangdong Province, China.
Abstract:
Neural precursor cell expressed developmentally down-regulated 4-like protein (NEDD4L), an E3 ubiquitin ligase, exerts an important role in diverse biological processes including development, tumorigenesis, and tumor progression. Although the role of NEDD4L in the pathogenesis of lung adenocarcinoma (LUAD) has been described, the mechanism by which NEDD4L promotes LUAD progression remains poorly understood. In the study, the correlation between NEDD4L level and clinical outcome in LUAD patients was analysed using the data from The Cancer Genome Atlas (TCGA) database. NEDD4L expression in LUAD cell lines and tissue samples was assessed through quantitative real-time PCR (qRT-PCR). The biological function of NEDD4L on regulating LUAD cell proliferation was tested with Cell Counting Kit-8 (CCK-8) assay in vitro, and mouse xenograft tumor model in vivo. We found that NEDD4L expression was significantly decreased in LUAD tissues and cell lines. Lower expression of NEDD4L exhibited a significantly poorer overall survival. Functionally, NEDD4L knockdown in H1299 cells accelerated cell growth, whereas NEDD4L overexpression in A549 cells repressed cell proliferation. NEDD4L overexpression also inhibited tumor xenograft growth in vivo. Mechanistically, NEDD4L decreased the protein stability of notch receptor 2 (Notch2) through facilitating its ubiquitination and degradation by ubiquitin-proteasome system. Consequently, NEDD4L negatively regulated Notch signaling activation in LUAD cells, and RO4929097 (a Notch inhibitor) treatment effectively repressed the effect of NEDD4L knockdown on LUAD cell proliferation. Taken together, these results demonstrate that down-regulated NEDD4L facilitates LUAD progression by activating Notch signaling, and NEDD4L may be a promising target to treat LUAD.
Insights
Neural precursor cell expressed developmentally down-regulated 4-like protein (NEDD4L) is decreased in lung adenocarcinoma (LUAD), promoting tumor progression by activating Notch signaling. Lower NEDD4L levels correlate with poorer survival in LUAD patients.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Neural precursor cell expressed developmentally down-regulated 4-like protein (NEDD4L) is an E3 ubiquitin ligase involved in development and tumorigenesis.
- While NEDD4L's role in lung adenocarcinoma (LUAD) is noted, its precise mechanism in promoting LUAD progression is unclear.
Purpose of the Study:
- To investigate the role of NEDD4L in LUAD progression and its underlying mechanism.
- To analyze the correlation between NEDD4L expression and clinical outcomes in LUAD patients.
Main Methods:
- Analysis of NEDD4L expression in LUAD tissues and cell lines using quantitative real-time PCR (qRT-PCR).
- Correlation analysis with clinical outcomes using The Cancer Genome Atlas (TCGA) database.
- In vitro (Cell Counting Kit-8 assay) and in vivo (mouse xenograft) functional studies of NEDD4L in LUAD cell proliferation.
- Investigation of NEDD4L's effect on Notch receptor 2 (Notch2) stability and Notch signaling pathway activation.
Main Results:
- NEDD4L expression was significantly decreased in LUAD tissues and cell lines, with lower levels correlating with poorer overall survival.
- NEDD4L knockdown accelerated LUAD cell proliferation in vitro and tumor growth in vivo, while overexpression inhibited proliferation and tumor growth.
- NEDD4L reduced Notch2 protein stability via ubiquitination and proteasomal degradation, thereby inhibiting Notch signaling.
- Notch pathway inhibition counteracted the pro-proliferative effects of NEDD4L knockdown.
Conclusions:
- Down-regulated NEDD4L facilitates LUAD progression by activating the Notch signaling pathway.
- NEDD4L acts as a tumor suppressor in LUAD and represents a potential therapeutic target for LUAD treatment.
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