» Articles » PMID: 31205519

Deleted in Breast Cancer 1 As a Novel Prognostic Biomarker for Digestive System Cancers: A Meta-Analysis

Overview
Journal J Cancer
Specialty Oncology
Date 2019 Jun 18
PMID 31205519
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Deleted in Breast Cancer 1 (DBC1/CCAR2) is a regulatory protein involved in cell survival and cancer progression. Herein, we focused on summarizing the overall prognostic value of DBC1 for digestive system cancers. Therefore, we conducted a meta-analysis based on 9 studies with 2391 patients to generated combined hazard ratios (HR) or odds ratio (OR) with its 95% confidence intervals (CI) for overall survival (OS) and clinicopathological features. Positive DBC1 expression was significantly associated with poor OS of digestive system cancers (pooled HR=1.650, 95% CI=1.087-2.504, P<0.019). Stratified analysis also verified the potential prognostic prediction of DBC1 in some subgroups, such as digestive tract cancers (pooled HR=1.685, 95% CI=1.013-2.802, P=0.044), univariate analysis method (pooled HR=2.077, 95%CI=1.221-3.533, P=0.007), publication date within five years (pooled HR=1.609, 95%CI=1.097-2.358, P =0.015), study sample size smaller than 200 (pooled HR=2.304, 95%CI=1.716-3.093, P<0.001) and cutoff value for positive tumor cells more than 50% (pooled HR=1.944, 95% CI=1.479-2.556, P<0.001). Additionally, in terms of the association between DBC1 expression and clinicopathological characteristics, DBC1 expression was correlated to age (pooled OR=0.596, 95%CI =0.467-0.761, P<0.001), WHO classification (pooled OR =3.780, 95% CI=2.303-6.205, P <0.001), Lauren classification (pooled OR=2.000, 95%CI =1.492-2.680, P<0.001), and lymph node metastasis (pooled OR=0.405, 95%CI=0.203-0.806, P=0.010). In conclusion, DBC1 could not only be an independent prognostic factor for survival of patients with digestive system cancer, but might also be a novel target for cancer therapy.

Citing Articles

Mechanistic insights into the dual role of CCAR2/DBC1 in cancer.

Kim H, Moon S, Kim J Exp Mol Med. 2023; 55(8):1691-1701.

PMID: 37524873 PMC: 10474295. DOI: 10.1038/s12276-023-01058-1.

References
1.
Tajima Y, Nakanishi Y, Ochiai A, Tachimori Y, Kato H, Watanabe H . Histopathologic findings predicting lymph node metastasis and prognosis of patients with superficial esophageal carcinoma: analysis of 240 surgically resected tumors. Cancer. 2000; 88(6):1285-93. View

2.
Hamaguchi M, Meth J, von Klitzing C, Wei W, Esposito D, Rodgers L . DBC2, a candidate for a tumor suppressor gene involved in breast cancer. Proc Natl Acad Sci U S A. 2002; 99(21):13647-52. PMC: 129730. DOI: 10.1073/pnas.212516099. View

3.
Kitajima K, Fujimori T, Fujii S, Takeda J, Ohkura Y, Kawamata H . Correlations between lymph node metastasis and depth of submucosal invasion in submucosal invasive colorectal carcinoma: a Japanese collaborative study. J Gastroenterol. 2004; 39(6):534-43. DOI: 10.1007/s00535-004-1339-4. View

4.
Kuzmichev A, Margueron R, Vaquero A, Preissner T, Scher M, Kirmizis A . Composition and histone substrates of polycomb repressive group complexes change during cellular differentiation. Proc Natl Acad Sci U S A. 2005; 102(6):1859-64. PMC: 548563. DOI: 10.1073/pnas.0409875102. View

5.
Ota H, Tokunaga E, Chang K, Hikasa M, Iijima K, Eto M . Sirt1 inhibitor, Sirtinol, induces senescence-like growth arrest with attenuated Ras-MAPK signaling in human cancer cells. Oncogene. 2005; 25(2):176-85. DOI: 10.1038/sj.onc.1209049. View