Expression of CXCR4 and CXCR7 in papillary thyroid carcinoma and adjacent tissues and their relationship with pathologic indicators of tumor aggressiveness

Endocr J. 2022 Feb 28;69(2):189-197. doi: 10.1507/endocrj.EJ21-0076. Epub 2021 Sep 28.

Abstract

The receptors of chemokines play a significance role in the aggressiveness of tumor. CXCR4/CXCR7 promote metastasis of papillary thyroid carcinoma (PTC). This study examined the expresssion of chemokine receptors CXCR4/CXCR7 in human tissue specimens of PTC and peritumoral nonmalignant tissues. The correlation between CXCR4/CXCR7 and the clinicopathological factors in PTC was also determined. CXCR4/CXCR7 were examined in 115 PTC tissues from 115 patients using immunohistochemistry. Staining intensity was compared with patients and tumor characteristics including gender, age, tumor size, capsule invasion, multifocality, lymph node metastasis, and nature of paracancerous tissue. [Statistics: rank sum test, Spearman rank order correlation test; p < 0.05]. Higher expression rates of CXCR4/CXCR7 exhibited in PTC compared with peritumoral nonmalignant tissues. The expression of them was correlated in cancer and paracancerous specimens. A trend toward higher CXCR4/CXCR7 expression was found among tumors showing positive lymph nodes and capsule invasion, while no association with sex, age, tumor size, and nature of paracancerous tissue. Number of lymph nodes was associated with higher intensity IHC staining for CXCR4/CXCR7. Intense staining for CXCR4 was also associated with multifocality. Expression of CXCR4/CXCR7 by PTCs was correlated with lymph node metastasis and capsule invasion. Although multiple bias, they were thought to play a significance role in the aggressiveness of PTC, which provides potential targets for therapeutic interventions.

Keywords: CXCR4; CXCR7; Chemokine receptors; Metastasis; Papillary thyroid carcinoma.

MeSH terms

  • Humans
  • Lymph Nodes / pathology
  • Lymphatic Metastasis / pathology
  • Receptors, CXCR
  • Receptors, CXCR4
  • Signal Transduction
  • Thyroid Cancer, Papillary / pathology
  • Thyroid Neoplasms* / pathology

Substances

  • ACKR3 protein, human
  • CXCR4 protein, human
  • Receptors, CXCR
  • Receptors, CXCR4