HOXA11 promotes lymphatic metastasis of gastric cancer via transcriptional activation of TGFβ1

作者：Li, Zhenyuan; Lu, Tailiang; Chen, Zhian; Yu, Xiang; Wang, Lingzhi; Shen, Guodong; Huang, Huilin; Li, Zhenhao; Ren, Yingxin; Guo, Weihong^*; Hu, Yanfeng^*

来源：iScience, 2023, 26(8): 107346.

DOI：10.1016/j.isci.2023.107346

• EPITHELIAL-MESENCHYMAL TRANSITION
• TUMOR LYMPHANGIOGENESIS
• NODE-METASTASIS
• HOMEOBOX GENES
• BLADDER-CANCER
• VEGF-C
• MECHANISMS
• EXPRESSION
• METHYLATION
• PROGRESSION

Most gastric cancer (GC) patients with early stage often have no lymph node (LN) metastases, while LN metastases appear in the advanced stage. However, there are some patients who present with early stage LN metastases and no LN metastases in the advanced stage. To explore the deeper molecular mechanisms involved, we collected clinical samples from early and advanced stage GC with and without LN metastases, as well as metastatic lymph nodes. Herein, we identified a key target, HOXA11, that was upregulated in GC tissues and closely associated with lymphatic metastases. HOXA11 transcriptionally regulates TGF beta 1 expression and activates the TGF beta 1/Smad2 pathway, which not only promotes EMT development but also induces VEGF-C secretion and lymphangiogenesis. These findings provide a plausible mechanism for HOXA11-modulated tumor in lymphatic metastasis and suggest that HOXA11 may represent a potential therapeutic target for clinical intervention in LN-metastatic gastric cancer.

• 单位
  1; 南方医科大学