1. Academic Validation
  2. Clinical significance of novel costimulatory molecule B7-H6 in human breast cancer

Clinical significance of novel costimulatory molecule B7-H6 in human breast cancer

  • Oncol Lett. 2017 Aug;14(2):2405-2409. doi: 10.3892/ol.2017.6417.
Jing Sun 1 Hong Tao 1 Xiaoning Li 1 Lu Wang 2 Jie Yang 1 Pingping Wu 1 Yaqin Zhang 1 Yundi Guo 1
Affiliations

Affiliations

  • 1 Institute of Medical Biotechnology, Suzhou Vocational Health College, Suzhou, Jiangsu 215009, P.R. China.
  • 2 Department of Pathology, The Fourth Affiliated Hospital of Nanjing Medical University, Suzhou, Jiangsu 214062, P.R. China.
Abstract

B7 homolog 6 (B7-H6), a member of the B7 family, is as a cell-surface ligand for natural cytotoxicity triggering receptor 3, which is expressed on natural killer cells. It has previously been reported that B7-H6 is undetectable in normal human tissues but is expressed on tumor cells. However, there are few studies focusing on the clinical significance of B7-H6 expression in human carcinoma, with the exception of three studies on ovarian, lung and gastric Cancer. The present study investigated the expression of B7-H6 protein in pathologic tissue samples from 305 patients with breast Cancer using immunohistochemistry. A high B7-H6 expression level was identified in tissues from 32.13% of patients with breast Cancer. These patients were revealed to also exhibit a high expression level of human epidermal growth factor receptor 2, a shorter survival time and a higher rate of lymph node metastasis. Furthermore, the expression level of B7-H6 was not associated with patient age, breast Cancer subtype, tumor size, tumor location or Estrogen Receptor expression. The results of the present study revealed that higher B7-H6 expression level in breast Cancer tissues was positively associated with tumor progression. This indicates that B7-H6 is associated with the progression and immunoevasion of human breast cancer; however, the molecular mechanisms underlying this potential effect require further investigation.

Keywords

B7 homolog 6; costimulatory molecule; human breast cancer; natural cytotoxicity triggering receptor 3.

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