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DOI 10.1136/jclinpath-2017-204872

Медицинская библиотека · Journal of clinical pathology · 2018

Clinical significance of FAP-α on microvessel and lymphatic vessel density in lung squamous cell carcinoma.

Chen Ling, Chen Meihui, Han Zenglei, Jiang Fengxing, Xu Chunyuan, Qin Yue, Ding Ning, Liu Yang, Zhang Tenglong, An Zhijie, Guo Chengye

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Аннотация

AIMS: We aimed to determine whether cancer-associated fibroblasts (CAFs) are associated with microvessel density (MVD) and lymphatic vessel density (LVD) in lung squamous cell carcinoma, as well as their clinical significance in predicting survival.

METHODS

122 patients were enrolled in the study. Samples were obtained on resection at the Department of Thoracic Surgery of the Qingdao Municipal Hospital between January 2011 and December 2014. Immunohistochemistry was used to determine vessel and lymphatic vessel density, and CAF abundance (fibroblast activation protein α (FAP-α) positivity). Statistical analyses were performed on 85 patients to test for correlation of CAF density and other clinicopathological variables with 3-year overall survival (OS) and disease-free survival (DFS).

RESULTS

High stromal CAF abundance significantly correlated with increased MVD and LVD in lung squamous cell carcinoma (p<0.05). χ2 test revealed a significant association of CAF density with lymph node metastasis. Cox proportional hazards model showed that both higher CAF density and lymph node metastasis negatively correlate with survival. CAF density or lymph node status can be used as an independent prognostic factor to predict 3-year OS and DFS.

CONCLUSIONS

CAF density, identified by FAP-α staining pattern, should be considered as a novel biomarker for disease prognosis in patients with lung squamous cell carcinoma.

Для цитирования: Chen Ling, Chen Meihui, Han Zenglei, Jiang Fengxing, Xu Chunyuan, Qin Yue, Ding Ning, Liu Yang, Zhang Tenglong, An Zhijie, Guo Chengye. Clinical significance of FAP-α on microvessel and lymphatic vessel density in lung squamous cell carcinoma.. Journal of clinical pathology. 2018. DOI: 10.1136/jclinpath-2017-204872.

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