Prognostic Value of GPNMB, EGFR, p-PI3K, and Ki-67 in Patients with Esophageal Squamous Cell Carcinoma

Author:

Wang Bo12,Li Mengyan13,Su Anna4,Gao Yongmei1,Shi Yan5,Li Chao6,Liu Wenying7,Su Liping1,Li Wan1,Ma Yuqing1ORCID

Affiliation:

1. Department of Pathology, The First Affiliated Hospital, Xinjiang Medical University, Urumqi, Xinjiang, China

2. Xinjiang Medical University, Urumqi, Xinjiang, China

3. Department of Pathology, Gem Flower Hospital, Changji, Xinjiang, China

4. Internal Medicine, Urumqi First People's Hospital, Urumqi, Xinjiang, China

5. Department of Pathology, Baoji Traditional Chinese Medicine Hospital, Baoji, Xian, China

6. Department of RICU, The First Affiliated Hospital, Xinjiang Medical University, Urumqi, Xinjiang, China

7. National Cancer Center/National Cancer Clinical Medical Research Center/Cancer Hospital, Hebei Chinese Academy of Medical Sciences, Langfang, Hebei, China

Abstract

Background. GPNMB is a newly discovered tumour-promoting factor that may promote tumour cell progression by activating the PI3K/AKT pathway by EGFR. However, there are insufficient studies about GPNMB in ESCC. This study investigated the relationship between GPNMB and EGFR/PI3K pathway genes in ESCC. Methods. The expression levels of GPNMB, EGFR, p-PI3K, and Ki-67 were examined using immunohistochemistry. Statistical analysis was done by SPSS 22.0 and R. Results. GPNMB mRNA expression is higher in ESCC compared with paracancerous tissues. The expression of EGFR, PIK3CA, PIK3CB, and AKT1 was increased in GPNMB upregulated samples. GPNMB expression was positively correlated with EGFR, p-PI3K, and Ki-67 expression. GPNMB was expressed higher in the AJCC III stage, lymph node metastasis, and moderately poorly differentiated patients. EGFR was higher expressed in patients with vascular invasion; p-PI3K expression in Kazak was higher than that in Han; Ki-67 expression was higher in tumour size 3 cm . Patients with high expression of GPNMB, p-PI3K, and Ki-67 had worse OS. p-PI3K, Ki-67, nerve invasion, and lymphatic metastasis were independent risk factors, and postoperative adjuvant therapy was a protective factor in ESCC. Conclusion. As a tumour-promoting factor, GPNMB is expected to be a potential target for ESCC.

Funder

Xinjiang Uygur Autonomous Region Youth Science and Technology Talent Project

Publisher

Hindawi Limited

Subject

Cancer Research,Cell Biology,Molecular Medicine,General Medicine,Pathology and Forensic Medicine

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