Cancer-associated fibroblast-derived WNT5A promotes cell proliferation, metastasis, stemness and glycolysis in gastric cancer via regulating HK2
Yongsu Xu, Zhengju Ren, Fang Zeng, Huan Yang, Chengju Hu

TL;DR
This study shows that cancer-associated fibroblasts boost gastric cancer progression by increasing WNT5A and HK2 activity.
Contribution
The novel finding is that CAF-derived WNT5A promotes GC progression by regulating HK2.
Findings
CAFs enhance GC cell proliferation, metastasis, stemness, and glycolysis.
WNT5A knockdown in CAFs or GC cells reduces tumor progression.
WNT5A promotes HK2 expression, which reverses the effects of WNT5A knockdown.
Abstract
Gastric cancer (GC) is one of the most common cancers worldwide. Tumor microenvironment plays an important role in tumor progression. This study aims to explore the role of cancer-associated fibroblasts (CAFs) in GC and the underlying mechanism. Cell viability, proliferation, invasion and migration were assessed by MTT, EdU, transwell and wound healing assays, respectively. Sphere formation assay was used to evaluate cell stemness. Glucose consumption, lactate production and ATP consumption were measured to assess glycolysis. In addition, The RNA and protein expression were detected by qRT-PCR and western blot. The interaction between wingless Type MMTV Integration Site Family, Member 5 A (WNT5A) and hexokinase 2 (HK2) was verified by Co-immunoprecipitation. The xenograft model was established to explore the function of CAFs on GC tumor growth in vivo. CAFs promoted the proliferation,…
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Taxonomy
TopicsWnt/β-catenin signaling in development and cancer · Pancreatic function and diabetes · Galectins and Cancer Biology
