Department of Radiation Oncology, Zhongshan Hospital Affiliated by Xiamen University, Xiamen, Fujian, China.
Department of Abdominal Surgery, The Cancer Hospital Affiliated by Guangzhou Medical University, Guangzhou, Guangdong, China.
Sci Rep. 2019 Sep 10;9(1):12973. doi: 10.1038/s41598-019-49480-8.
As a key glycolysis enzyme, the significance of pyruvate dehydrogenase kinase 1 (PDK1) in the development of colorectal cancer (CRC) remains unknown. This study revealed that the prognosis of CRC patients with high levels of PDK1 was poor, and PDK1 knockdown significantly reduced liver metastasis of CRC in both nude mice and immune competent BALB/C mice. When combined with cryptotanshinone (CPT), an inhibitor of STAT3-p-Y705, the liver metastasis was further inhibited. PDK1 knockdown obviously increased reactive oxygen species level in anoikis conditions and subsequently resulted in an elevated anoikis, but the combination of PDK1 knockdown and CPT showed a reduced effect on anoikis. Based on this discrepancy, the adherence ability of CRC cells to matrix protein fibronectin was further detected. It showed that PDK1 knockdown significantly decreased the adherence of CRC cells to fibronectin when combined with CPT. These results suggest that inhibition of PDK1 can decrease the surviving CRC cells in blood circulation via up-regulation of anoikis, and inhibition of STAT3-p-Y705 can prevent it to settle down on the liver premetastatic niche, which ultimately reduces liver metastasis.
作为一种关键的糖酵解酶,丙酮酸脱氢酶激酶 1(PDK1)在结直肠癌(CRC)发展中的意义尚不清楚。本研究表明,PDK1 水平高的 CRC 患者预后较差,PDK1 敲低显著减少了裸鼠和免疫功能正常的 BALB/C 小鼠 CRC 的肝转移。当与 STAT3-p-Y705 的抑制剂隐丹参酮(CPT)联合使用时,肝转移进一步受到抑制。PDK1 敲低在无锚定条件下明显增加了活性氧水平,随后导致凋亡增加,但 PDK1 敲低和 CPT 的联合使用对凋亡的抑制作用降低。基于这一差异,进一步检测了 CRC 细胞对基质蛋白纤维连接蛋白的黏附能力。结果表明,PDK1 敲低与 CPT 联合使用时,显著降低了 CRC 细胞对纤维连接蛋白的黏附。这些结果表明,抑制 PDK1 可以通过上调凋亡来减少循环血液中存活的 CRC 细胞,而抑制 STAT3-p-Y705 可以防止其在肝转移前微环境中定居,从而最终减少肝转移。