Clinical implication of leucine zipper/EF hand-containing transmembrane-1 overexpression in the prognosis of triple-negative breast cancer

被引:17
作者
Wang, Chang-an [1 ]
Liu, Qixiang [1 ,2 ]
Chen, Yunbo [1 ]
Liu, Shuangping [2 ]
Xu, Jingwei [1 ]
Cui, Xuelian [2 ]
Zhang, Yan [1 ]
Piao, Longzhen [3 ]
机构
[1] Jilin Univ, Dept Breast Surg, Hosp 2, Changchun 130041, Peoples R China
[2] Yanbian Univ, Dept Pathol, Coll Med, Yanji 133002, Peoples R China
[3] Yanbian Univ Hosp, Dept Oncol, Yanji 133000, Peoples R China
关键词
Triple negative breast cancer; LETM1; Prognosis; Biomarker; WOLF-HIRSCHHORN-SYNDROME; LETM1; PROTEIN; ASSOCIATION; EXPRESSION; CARCINOMA; FEATURES; ENCODES; BRCA1;
D O I
10.1016/j.yexmp.2014.12.012
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Triple negative breast cancer (TNBC) is a heterogeneous disease with higher rates of relapse and decreased overall survival in metastatic tumors. Due to its poor prognosis, it is necessary to identify effective biomarkers that are associated with tumor growth and metastasis. The leucine zipper/EF hand-containing transmembrane-1 (LETM1) protein, which is a mitochondrial inner membrane protein, can reduce mitochondrial biogenesis and ATP production. The expression levels of LETM1 were significantly increased in numerous human malignancies. However, the clinicopathological characteristics and prognostic value of LETM1 overexpression in TNBC remains unclear. LETM1 protein was detected in 107 TNBC, 42 ductal carcinoma in situ (DCIS) and 65 adjacent non-tumor breast tissues using immunohistochemical (IHC) staining. Immunofluorescence (IF) staining was also performed to detect the localization of LETM1 protein in MCF-7 BC cells. The correlations between LETM1 overexpression and clinicopathological features of TNBC were evaluated using Chi-squared test and Fisher's exact tests. The survival rate was calculated using the Kaplan-Meier method. LETM1 protein showed cytoplasmic staining patterns in TNBC. The strongly positive rate of LETM1 in TNBC was 69.2% (74/107), which was significantly higher than in both DCIS 35.7% (15/42) and adjacent non-tumor tissues 12.3% (8/65). High-level expression of LETM1 was positively correlated with late clinical stage, poor differentiation, lymph node metastasis, disease-free survival (DFS) and 10-year overall survival (OS) rates in TNBC. Further analysis showed that high LETM1 expression along with clinical stage emerged as significant independent risk factors in patients with TNBC. In conclusion, LETM1 protein overexpression is associated with TNBC progression, and may be a potential biomarker for poor prognostic evaluation of TNBC. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:254 / 259
页数:6
相关论文
共 28 条
  • [1] Descriptive analysis of estrogen receptor (ER)negative, progesterone receptor (PR)-negative, and HER2-negative invasive breast cancer, the so-called triple-negative phenotype - A population-based study from the California Cancer Registry
    Bauer, Katrina R.
    Brown, Monica
    Cress, Rosemary D.
    Parise, Carol A.
    Caggiano, Vincent
    [J]. CANCER, 2007, 109 (09) : 1721 - 1728
  • [2] Triple-negative breast cancer: Molecular features, pathogenesis, treatment and current lines of research
    Bosch, Ana
    Eroles, Pilar
    Zaragoza, Rosa
    Vina, Juan R.
    Lluch, Ana
    [J]. CANCER TREATMENT REVIEWS, 2010, 36 (03) : 206 - 215
  • [3] High Expression of Leucine Zipper-EF-Hand Containing Transmembrane Protein 1 Predicts Poor Prognosis in Head and Neck Squamous Cell Carcinoma
    Chen, Liyan
    Yang, Yang
    Liu, Shuangping
    Piao, Longzhen
    Zhang, Yuan
    Lin, Zhenhua
    Li, Zhuhu
    [J]. BIOMED RESEARCH INTERNATIONAL, 2014, 2014
  • [4] Triple-negative breast cancer: Clinical features and patterns of recurrence
    Dent, Rebecca
    Trudeau, Maureen
    Pritchard, Kathleen I.
    Hanna, Wedad M.
    Kahn, Harriet K.
    Sawka, Carol A.
    Lickley, Lavina A.
    Rawlinson, Ellen
    Sun, Ping
    Narod, Steven A.
    [J]. CLINICAL CANCER RESEARCH, 2007, 13 (15) : 4429 - 4434
  • [5] Drugs targeting mitochondrial functions to control tumor cell growth
    Dias, N
    Bailly, C
    [J]. BIOCHEMICAL PHARMACOLOGY, 2005, 70 (01) : 1 - 12
  • [6] LETM1, deleted in Wolf-Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability
    Dimmer, Kai Stefan
    Navoni, Francesca
    Casarin, Alberto
    Trevisson, Eva
    Endele, Sabine
    Winterpacht, Andreas
    Salviati, Leonardo
    Scorrano, Luca
    [J]. HUMAN MOLECULAR GENETICS, 2008, 17 (02) : 201 - 214
  • [7] LETM1, a novel gene encoding a putative EF-hand Ca2+-binding protein, flanks the Wolf-Hirschhorn syndrome (WHS) critical region and is deleted in most WHS patients
    Endele, S
    Fuhry, M
    Pak, SJ
    Zabel, BU
    Winterpacht, A
    [J]. GENOMICS, 1999, 60 (02) : 218 - 225
  • [8] Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008
    Ferlay, Jacques
    Shin, Hai-Rim
    Bray, Freddie
    Forman, David
    Mathers, Colin
    Parkin, Donald Maxwell
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2010, 127 (12) : 2893 - 2917
  • [9] Triple-Negative Breast Cancer
    Foulkes, William D.
    Smith, Ian E.
    Reis-Filho, Jorge S.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (20) : 1938 - 1948
  • [10] LETM1 haploinsufficiency causes mitochondrial defects in cells from humans with Wolf-Hirschhorn syndrome: implications for dissecting the underlying pathomechanisms in this condition
    Hart, Lesley
    Rauch, Anita
    Carr, Antony M.
    Vermeesch, Joris R.
    O'Driscoll, Mark
    [J]. DISEASE MODELS & MECHANISMS, 2014, 7 (05) : 535 - 545