Decreased expression of Beclin-1 and LC3 in human lung cancer

被引:76
作者
Jiang, Zi-Feng [1 ]
Shao, Li-Jie [1 ]
Wang, Wei-Min [1 ]
Yan, Xue-Bo [1 ]
Liu, Rong-Yu [1 ]
机构
[1] Anhui Med Univ, Dept Pulm, Anhui Geriatr Inst, Affiliated Hosp 1, Hefei, Peoples R China
关键词
Autophagy; Beclin-1; LC3; Expression; Lung cancer; DOUBLE-EDGED-SWORD; AUTOPHAGOSOME MARKER; PRONE PROTEINS; APOPTOSIS; DISEASE; INHIBITION; HOMOLOG; HEALTH; TISSUE; CELLS;
D O I
10.1007/s11033-011-0734-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autophagy, a conversed response to stress, has recently been studied in human cancers. Two important autophagic genes-Beclin-1 and LC3 are reported in several human cancers. However, the expressions of Beclin-1 and LC3 in lung cancer have not yet been investigated. In the present study, we investigated the expression of Beclin-1 and LC3, and the relationship between the expression profile and the clinical or pathological changes in human lung cancer. 40 primary lung cancer patients are involved in present study. mRNA expressions of Beclin-1 and LC3-II were detected by Real Time PCR and the protein levels were assessed by immunohistochemistry and western blot. Relative lower expressions of Beclin-1 and LC3-II mRNA were found in the lung cancer tissues compared to counterpart normal tissues. Consistently, the lower amount of Beclin-1 and LC3-II protein was found in lung cancer tissues. However, the expressions of Beclin-1 and LC3-II in lung cancer tissues were not affected by patients' age, gender, smoking, histological type, lymph node metastasis and tumor-node-metastasis (TNM) stage. Both mRNA and protein levels of Beclin-1 and LC3-II were significantly decreased in lung cancer tissues which suggested that autophagy may be involved in the pathogenesis of lung cancer.
引用
收藏
页码:259 / 267
页数:9
相关论文
共 43 条
[1]   Inhibition of macroautophagy triggers apoptosis [J].
Boya, P ;
González-Polo, RA ;
Casares, N ;
Perfettini, JL ;
Dessen, P ;
Larochette, N ;
Métivier, D ;
Meley, D ;
Souquere, S ;
Yoshimori, T ;
Pierron, G ;
Codogno, P ;
Kroemer, G .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (03) :1025-1040
[2]   The autophagosomal-lysosomal compartment in programmed cell death [J].
Bursch, W .
CELL DEATH AND DIFFERENTIATION, 2001, 8 (06) :569-581
[3]   BIOCHEMICAL METHODS TO MONITOR AUTOPHAGY-RELATED PROCESSES IN YEAST [J].
Cheong, Heesun ;
Klionsky, Daniel J. .
AUTOPHAGY: LOWER EUKARYOTES AND NON-MAMMALIAN SYSTEMS, PT A, 2008, 451 :1-26
[4]   Cancer Therapy Beyond Apoptosis Autophagy and Anoikis as Mechanisms of Cell Death [J].
Coates, Jodi M. ;
Galante, Joseph M. ;
Bold, Richard J. .
JOURNAL OF SURGICAL RESEARCH, 2010, 164 (02) :301-308
[5]   Apoptosis and autophagy: Targeting autophagy signalling in cancer cells -'trick or treats'? [J].
Corcelle, Elisabeth A. ;
Puustinen, Pietri ;
Jaattela, Marja .
FEBS JOURNAL, 2009, 276 (21) :6084-6096
[6]   Cross talk between apoptosis and autophagy by caspase-mediated cleavage of Beclin 1 [J].
Djavaheri-Mergny, M. ;
Maiuri, M. C. ;
Kroemer, G. .
ONCOGENE, 2010, 29 (12) :1717-1719
[7]   Defective autophagy leads to cancer [J].
Edinger, AL ;
Thompson, CB .
CANCER CELL, 2003, 4 (06) :422-424
[8]   Autophagy: A lysosomal degradation pathway with a central role in health and disease [J].
Eskelinen, Eeva-Liisa ;
Saftig, Paul .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2009, 1793 (04) :664-673
[9]   LC3-I conversion to LC3-II does not necessarily result in complete autophagy [J].
Gimenez-Xavier, Pol ;
Francisco, Roser ;
Platini, Francesca ;
Perez, Ricardo ;
Ambrosio, Santiago .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2008, 22 (06) :781-785
[10]   LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing [J].
Kabeya, Y ;
Mizushima, N ;
Uero, T ;
Yamamoto, A ;
Kirisako, T ;
Noda, T ;
Kominami, E ;
Ohsumi, Y ;
Yoshimori, T .
EMBO JOURNAL, 2000, 19 (21) :5720-5728