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Loss of ß-arrestin-2 and Activation of CXCR2 Correlate with Lymph Node Metastasis in Non-small Cell Lung Cancer.
Cong, Lei; Qiu, Zhi-Yong; Zhao, Yang; Wang, Wei-Bo; Wang, Cai-Xia; Shen, Hong-Chang; Han, Jun-Qing.
Afiliación
  • Cong L; Department of Oncology, Shandong Provincial Hospital Affiliated to Shandong University, #324 Jingwu Road, Jinan 250021, P.R.China.
  • Qiu ZY; Department of Oncology, Shandong Provincial Hospital Affiliated to Shandong University, #324 Jingwu Road, Jinan 250021, P.R.China.
  • Zhao Y; Department of Breast Surgery, Key Laboratory of Breast Cancer in Shanghai, Collaborative Innovation Center of Cancer Medicine, Fudan University Shanghai Cancer Center, Shanghai, 200030, China.
  • Wang WB; Department of Oncology, Shanghai Medicine College, Fudan University, Shanghai, 200030, China.
  • Wang CX; Department of Oncology, Shandong Provincial Hospital Affiliated to Shandong University, #324 Jingwu Road, Jinan 250021, P.R.China.
  • Shen HC; Department of Oncology, Shandong Provincial Hospital Affiliated to Shandong University, #324 Jingwu Road, Jinan 250021, P.R.China.
  • Han JQ; Department of Oncology, Shandong Provincial Hospital Affiliated to Shandong University, #324 Jingwu Road, Jinan 250021, P.R.China.
J Cancer ; 8(14): 2785-2792, 2017.
Article en En | MEDLINE | ID: mdl-28928867
ABSTRACT

Background:

Although ß-arrestin-2 (ß-arr2) and CXCR2 have been shown to affect various malignant tumors, their exact roles in lung cancer remain unclear. We investigated expression of ß-arr2 and CXCR2 in patients with non-small cell lung cancer (NSCLC) and their correlation with lymph node metastasis and prognosis.

Methods:

We reviewed medical records of 136 patients with NSCLC who underwent surgical resection, and assessed their specimens immunohistochemically for expression of ß-arr2 and CXCR2 in primary tumors and metastatic lymph nodes (MLNs), respectively.

Results:

High ß-arr2 expression was seen in 63 specimens (46.3%), and was significantly associated with male patients (P=0.011), squamous cell carcinoma (P=0.003), and lymph node metastasis (P<0.001). High CXCR2 expression was seen in 62 specimens (45.6%), and was significantly correlated only with lymph node metastasis (P<0.001). Expression of ß-arr2 was significantly lower at MLNs than at primary lesions (Z=-2.315; P=0.021; Wilcoxon signed-rank), whereas CXCR2 expression was significantly higher in MLNs than in primary lesions (Z=-3.712; P<0.001; Wilcoxon signed-rank). No relationship was seen between ß-arr2 and CXCR2 expression in primary lesions (r=-0.065, P=0.548; Spearman rank coefficient), but they were inversely related in MLNs (r=-0.263, P=0.012). Kaplan-Meier survival curve was shown that low ß-arr2 and high CXCR2 expressions was associated with poor survival (log-rank χ2=5.926, P=0.015).

Conclusions:

ß-arr2 may promote lymph node metastasis in NSCLC by modulating CXCR2 activation.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Cancer Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Cancer Año: 2017 Tipo del documento: Article
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