Annals of Coloproctology (Apr 2018)

Association Between c-Met and Lymphangiogenic Factors in Patients With Colorectal Cancer

  • Han Jo Kim,
  • Moo-Jun Baek,
  • Dong Hyun Kang,
  • Sang-Cheol Lee,
  • Sang Byung Bae,
  • Kyu Taek Lee,
  • Namsu Lee,
  • Hyungjoo Kim,
  • Dongjun Jeong,
  • Tae Sung Ahn,
  • Moon Soo Lee,
  • Dae Sik Hong,
  • Jong-Ho Won

DOI
https://doi.org/10.3393/ac.2017.10.10
Journal volume & issue
Vol. 34, no. 2
pp. 88 – 93

Abstract

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Purpose Animal models show a strong relationship between lymphangiogenesis and lymph node metastasis. However, the clinical significance of lymphangiogenesis in patients with colorectal cancer (CRC) remains uncertain. This study aimed to evaluate the association between c-Met and lymphangiogenic factors and to elucidate the prognostic significance of c-Met in patients with CRC. Methods A total of 379 tissue samples were obtained from surgically resected specimens from patients with CRC at Soonchunhyang University Cheonan Hospital between January 2002 and December 2010. The expressions of c-Met, vascular endothelial growth factor (VEGF)-C, VEGF-D, VEGF receptor (VEGFR)-3, and podoplanin were examined using immunohistochemistry. The expression of c-Met and clinical factors were analyzed. Results Of the 379 tissues, 301 (79.4%) had c-Met expression. High expression of c-Met in tumor cells was significantly associated with high expression of VEGF-C (P < 0.001) and VEGFR-3 (P = 0.001). However, no statistically significant association with podoplanin (P = 0.587) or VEGF-D (P = 0.096) was found. Of the 103 evaluable patients, expression of c-Met in tumor cells was significantly associated with advanced clinical stage (P = 0.020), positive lymph node status (P = 0.038), and high expression of VEGF-C (P = 0.020). However, no statistically significant association with podoplanin (P = 0.518), VEGFR-3 (P = 0.085), VEGF-D (P = 0.203), or overall survival (P = 0.360) was found. Conclusion Our results provide indirect evidence for an association and possible regulatory link of c-Met with the lymphangiogenic markers, but c-Met expression in patients with CRC is not a prognostic indicator for overall survival.

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