» Articles » PMID: 27432467

Expression and Clinical Significance of Apollon in Esophageal Squamous Cell Carcinoma

Overview
Journal Mol Med Rep
Specialty Molecular Biology
Date 2016 Jul 20
PMID 27432467
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Apollon, an unusually large member of the inhibitors of apoptosis protein family, may be important for oncogenesis development. The aim of the present study was to assess the association between esophageal squamous cell carcinoma (ESCC) and Apollon expression levels, and to highlight the association between Apollon and the occurrence, development and prognosis of ESCC. Apollon expression was detected by immunohistochemical staining and reverse transcription-quantitative polymerase chain reaction in ESCC tissues, adjacent non‑cancerous tissues and paired normal tissues respectively, in order to analyze the association between Apollon expression and the clinicopathological features of ESCC. Survival analysis was used to assess the prognostic significance of Apollon expression. It was determined that the mRNA and protein expression levels of Apollon were significantly higher in the carcinoma tissues compared with the adjacent non‑cancerous tissues and normal control tissues (P<0.001). There was a significant difference in lymph node involvement and the tumor, nodes, and metastases stage in patients categorized according to different Apollon expression levels. The prognostic significance of Apollon was also determined using the log‑rank method. The overexpression of Apollon was associated with shorter overall survival and disease-free survival rates. The present study indicates that Apollon expression is associated with the biological characteristics of ESCC, and may be a valuable prognostic factor and a novel chemotherapeutic target for ESCC treatment.

Citing Articles

Mechanisms of Drug Resistance in Ovarian Cancer and Associated Gene Targets.

Alatise K, Gardner S, Alexander-Bryant A Cancers (Basel). 2022; 14(24).

PMID: 36551731 PMC: 9777152. DOI: 10.3390/cancers14246246.


Oral Squamous Cell Carcinoma: The Role of BIRC6 Serum Level.

Banakar M, Torabi Ardekani S, Zare R, Malekzadeh M, Mirhadi H, Khademi B Biomed Res Int. 2022; 2022:5425478.

PMID: 36033570 PMC: 9410788. DOI: 10.1155/2022/5425478.


Targeting DNA Damage Response and Repair to Enhance Therapeutic Index in Cisplatin-Based Cancer Treatment.

Kiss R, Xia F, Acklin S Int J Mol Sci. 2021; 22(15).

PMID: 34360968 PMC: 8347825. DOI: 10.3390/ijms22158199.


Molecular Mechanisms of Chemotherapy Resistance in Head and Neck Cancers.

Kanno Y, Chen C, Lee H, Chiou J, Chen Y Front Oncol. 2021; 11:640392.

PMID: 34026617 PMC: 8138159. DOI: 10.3389/fonc.2021.640392.


A Combined Systemic Strategy for Overcoming Cisplatin Resistance in Head and Neck Cancer: From Target Identification to Drug Discovery.

Chen Y, You G, Lai M, Lu L, Chen C, Ting L Cancers (Basel). 2020; 12(11).

PMID: 33238517 PMC: 7700594. DOI: 10.3390/cancers12113482.


References
1.
Lerut T, Coosemans W, Decker G, De Leyn P, Nafteux P, Van Raemdonck D . Cancer of the esophagus and gastro-esophageal junction: potentially curative therapies. Surg Oncol. 2001; 10(3):113-22. DOI: 10.1016/s0960-7404(01)00027-5. View

2.
Ren J, Shi M, Liu R, Yang Q, Johnson T, Skarnes W . The Birc6 (Bruce) gene regulates p53 and the mitochondrial pathway of apoptosis and is essential for mouse embryonic development. Proc Natl Acad Sci U S A. 2005; 102(3):565-70. PMC: 543482. DOI: 10.1073/pnas.0408744102. View

3.
Lamers F, Schild L, Koster J, Speleman F, Ora I, Westerhout E . Identification of BIRC6 as a novel intervention target for neuroblastoma therapy. BMC Cancer. 2012; 12:285. PMC: 3495678. DOI: 10.1186/1471-2407-12-285. View

4.
Hauser H, Bardroff M, Pyrowolakis G, Jentsch S . A giant ubiquitin-conjugating enzyme related to IAP apoptosis inhibitors. J Cell Biol. 1998; 141(6):1415-22. PMC: 2132795. DOI: 10.1083/jcb.141.6.1415. View

5.
Livak K, Schmittgen T . Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods. 2002; 25(4):402-8. DOI: 10.1006/meth.2001.1262. View