Targeting the NAD+ salvage pathway suppresses APC mutation-driven colorectal cancer growth and Wnt/β-catenin signaling via increasing Axin level

Abstract

Background: The role and mechanism of the nicotinamide adenine dinucleotide (NAD +) salvage pathway in cancer cell proliferation is poorly understood. Nicotinamide phosphoribosyltransferase (NAMPT), which converts nicotinamide into NAD + , is the rate-limiting enzyme in the NAD + salvage pathway. Here, we assessed the role of NAMPT in the proliferation of colorectal cancer. Methods: Real-time PCR, immunohistochemistry, western blotting, and analyses of datasets from Oncomine and Gene Expression Omnibus were conducted to assess the expression of NAMPT at the mRNA and protein levels in colorectal cancer. The Kaplan Meier plotter online tool was used to evaluate the prognostic role of NAMPT. Knockdown of NAMPT was performed to assess the role of NAMPT in colorectal cancer cell proliferation and tumorigenesis both in vitro and in vivo. Overexpression of NAMPT was used to evaluate impact of NAMPT on colorectal cancer cell proliferation in vitro. NAD + quantitation, immunofluorescence, dual luciferase assay and western blot were used to explore the mechanism of colorectal cancer proliferation. Transwell migration and invasion assays were conducted to assess the role of NAMPT in cell migration and invasion abilities of colorectal cancer cells. Results: Our study indicated that the inhibition of NAMPT decreased proliferation capacity of colorectal cancer cells both in vitro and in vivo. Conversely, overexpression of NAMPT could promote cell proliferation in vitro. NAMPT inhibition induced β-catenin degradation by increasing Axin expression levels; this resulted in the inhibition of Wnt/ β-catenin signaling and cell proliferation in colorectal cancer. The addition of nicotinamide mononucleotide, the enzymatic product of NAMPT, effectively reversed β-catenin protein degradation and inhibited growth. Similarly, the knockdown of Axin also decreased the cell death induced by the inhibition of NAMPT. In addition, we showed that colorectal cancer tissues harbored significantly higher levels of NAMPT than the levels harbored by paired normal tissues, especially in colorectal cancer stages I and II. And the overexpression of NAMPT was associated with unfavorable survival results.

Mitochondrial Deoxyguanosine Kinase Regulates NAD+ Biogenesis Independent of Mitochondria Complex I Activity

“…Recently, accumulated evidence indicates that the NAD + biosynthesis pathway plays an important role in tumor progression and metastasis (22). Ye et al reported that targeting the NAD + salvage pathway suppressed APC mutationdriven colorectal cancer growth (23). Nicotinamide phosphoribosyl transferase (NAMPT), which is a rate-limiting enzyme for NAD + synthesis in the salvage pathway, was shown to be overexpressed in many types of cancer, suggesting that NAMPT acts as a regulator of cancer invasion and metastasis (7,24).…”

A Negative Feedback Loop Between NAMPT and TGF-β Signaling Pathway in Colorectal Cancer Cells

“… 29 Moreover, the Wnt/β-catenin pathway is involved in the functions of NAMPT during CRC proliferation. 30 …”

Diagnosis Accuracy and Prognostic Significance of the Dickkopf-1 Protein in Gastrointestinal Carcinomas: Systematic Review and Network Meta-analysis

“…The Wnt/β-catenin signalling cascade governs cell proliferation and cell fate during embryonic development and tissue homeostasis 7 - 8 . The Wnt/β-catenin signalling pathway is one of the most important pathways in the initiation and progression of GIC 9 - 10 . Currently, the biomarker DKK-1 is being studied and is highly expressed in various GIC 11 - 12 .…”