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Chinese Journal of Diagnostics(Electronic Edition) ›› 2015, Vol. 03 ›› Issue (04): 282-287. doi: 10.3877/cma.j.issn.2095-655X.2015.04.016

Special Issue:

• Clinical Study • Previous Articles     Next Articles

Expression of CXCL12/CXCR4, Topo Ⅱ α and NF-κB in tissues of triple negative breast carcinoma

Dongyu Hu1,(), Fangfang Xu2, Quanyi Wang3, Guangzhang Zhao4, Xinchang Jiang1   

  1. 1. Department of Oncology, Affiliated Hospital of Jining Medical University, Jining 272029, China
    2. Department of Pathology, The First People′s Hospital of Jining, Jining 272011, China
    3. Department of Pathology, Affiliated Hospital of Jining Medical University, Jining 272029, China
    4. Department of Breast Thyroid Surgery, Affiliated Hospital of Jining Medical University, Jining 272029, China
  • Received:2015-08-10 Online:2015-11-26 Published:2015-11-26
  • Contact: Dongyu Hu
  • About author:
    Corresponding author: Hu Dongyu, Email:

Abstract:

Objective

To explore the meaning of the expression of CXCL12/CXCR4, Topo Ⅱα, NF-κB in tissues of triple negative breast carcinoma (TNBC).

Methods

Fifty-three cases with TNBC were enrolled as TNBC group, and seventy-six cases with non-triple negative breast carcinoma (N-TNBC) as N-TNBC group.Immunohistochemical stainings were conducted with resection specimens, and proteins of CXCL12/CXCR4, Topo Ⅱ α, NF-κB were detected.Patients were followed up after surgery to record postoperative recurrence, metastasis and death.The death cases were recorded by censored data, and surviving cases were followed up for 3 years at least.Rates of recurrence and metastasis, mortality, and disease free survival time (DFS) were compared among different groups.

Results

Less than or equal to 50 years old, lymph node metastasis, invasive ductal carcinoma and Ⅲ stage were TNBC patients′ main features.Positive cells of CXCL12, CXCR4, Topo Ⅱ α, NF-κB were 66.04%, 84.91%, 69.81%, 79.25% respectively in TNBC group, and were 40.79%, 51.32%, 40.79%, 51.32% in N-TNBC group.Positive cells of CXCL12, CXCR4, Topo Ⅱ α, NF-κB in TNBC group were all higher than those in N-TNBC group (χ2=7.97, 15.51, 10.55, 10.43; P<0.05). Metastasis rate, mortality and DFS were 20.75%, 28.30%, (24.35±3.50)months respectively in TNBC group, and were 11.32%, 13.16%, (32.02±4.00)months in N-TNBC group.Metastasis rate, mortality in TNBC group were both greater than those in N-TNBC group (χ2=4.51, 4.58; P<0.05), yet DFS was less than that in N-TNBC group (t=5.29, P<0.05). Rates of recurrence and metastasis in positive expression groups of CXCL12, CXCR4, Topo Ⅱ α, NF-κB were 19.70%, 17.86%, 19.12%, 18.52%, and were 6.35%, 4.44%, 6.56%, 4.17% in negative expression groups, and they were all more significant than those in negative expression groups (χ2=5.02, 4.61, 4.43, 5.43; P<0.05). Mortality was 27.27%, 25.00%, 26.47%, 24.69% in positive expression groups, and was 11.11%, 8.89%, 11.48%, 10.42% in negative expression groups, and they were all bigger than those in negative expression groups (χ2=5.39, 4.87, 4.63, 3.93; P<0.05). DFS were (23.17±3.30)months, (24.50±3.21)months, (23.51±3.65)months, (25.36±3.65)months in positive expression groups, and were(32.25±3.55)months, (33.00±4.15)months, (35.00±5.10)months, (31.86±4.57)months in negative groups, and the differences between the two groups were statistically significant (t=5.37, 5.80, 6.21, 5.08; P<0.05).

Conclusion

There are high expression of CXCL12, CXCR4, Topo Ⅱ α, NF-κB in tissue of TNBC, with early recurrence and metastasis and poor prognosis, and it may be related with increasing tumor cells′ invasive ability and mediating specific metastasis of lymph node.

Key words: Breast neoplasms, Prognosis, Neoplasm invasiveness

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