LGR5 overexpression confers poor relapse-free survival in breast cancer patients

被引:33
|
作者
Hou, Ming-Feng [1 ,2 ,3 ]
Chen, Po-Ming [4 ]
Chu, Pei-Yi [5 ,6 ,7 ]
机构
[1] Kaohsiung Med Univ, Coll Med, Dept Surg, Kaohsiung, Taiwan
[2] Kaohsiung Municipal Hsiaokang Hosp, Dept Surg, Kaohsiung, Taiwan
[3] Kaohsiung Med Univ Hosp, Div Breast Surg, Kaohsiung, Taiwan
[4] Taiwan Agr Chem & Tox Subst Res Inst, Council Agr, Taichung, Taiwan
[5] Show Chwan Mem Hosp, Dept Pathol, 542,Sec 1,Chung Shang Rd, Changhua 50008, Changhua, Taiwan
[6] Fu Jen Catholic Univ, Coll Med, Sch Med, New Taipei, Taiwan
[7] Natl Hlth Res Inst, Natl Inst Canc Res, Tainan, Taiwan
关键词
Breast cancer; Cancer stem cell; LGR5; STEM-LIKE CELLS; LGR5-POSITIVE CELLS; EXPRESSION; COLON;
D O I
10.1186/s12885-018-4018-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Cancer stem cells (CSCs) are believed to promote the malignant transformation of breast cancer via multiple signaling pathways, including the Wnt/beta-catenin pathway. Leucine-rich repeat-containing G protein-coupled receptor 5 (LGR5) has been identified as a CSC-associated Wnt-regulated target gene, but its clinical significance in the context of breast cancer remains elusive. Therefore, the purpose of this study was to investigate the clinical significance of the LGR5-beta-catenin axis in breast cancer. Methods: Breast cancer tissue blocks from 126 patients were used to construct a tissue microarray (TMA). Histopathological and clinical data including age; tumor size; estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2) level; tumor grade; lymph node (LN) status; and survival were obtained from the cancer registry database and patients' medical records. Tissue on the breast TMA was scored for LGR5 and beta-catenin expression using semi-quantitative immunohistochemical (IHC) staining. We also analyzed LGR5 expression in cellular datasets available through ONCOMINE, a web-based cancer microarray database. Results: Immunohistochemical staining revealed that 58 tumors (46%) exhibited high LGR5 expression, whereas 56 tumors (47%) displayed high beta-catenin expression. High levels of LGR5 expression were significantly associated with tumor size (p = 0.002), LN metastasis status (p = 0.044), and triple-negative breast cancer (p = 0.029), consistent with our findings from the ONCOMINE database. In addition, we also found that beta-catenin - expressing breast cancers were positive correlated with HER2 overexpression. Finally, with respect to clinical outcomes, patients with high levels of LGR5-beta-catenin axis expression exhibited poorer relapse-free survival (RFS) compared to patients with low levels of LGR5-beta-catenin axis expression (p = 0.027). Conclusion: LGR5 overexpression was significantly associated with high T stage and LN metastasis status. High LGR5 expression was also associated with reduced RFS, indicating that LGR5 may represent a promising prognostic marker for breast cancer patients.
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页数:8
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