Integrase interactor 1 regulates proliferation, apoptosis and invasion in gastric cancer cells

被引:4
作者
Wang Xiao-chun [1 ]
Li Yong [1 ]
Fan Li-qiao [1 ]
Tan Bi-bo [1 ]
Li Zhong [1 ,2 ]
Liu Yu [1 ]
Zhang Zhi-dong [1 ]
机构
[1] Hebei Med Univ, Dept Gen Surg, Affiliated Hosp 4, Shijiazhuang 050011, Hebei, Peoples R China
[2] Hebei Univ, Dept Surg Oncol, Affiliated Hosp, Baoding 071000, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
integrase interactor 1; gastric neoplasm; proliferation; apoptosis; invasion; MALIGNANT RHABDOID TUMOR; SOFT-TISSUE SARCOMAS; SMARCB1/INI1; PROTEIN; EPITHELIOID SARCOMA; CYCLE ARREST; SUPPRESSOR; EXPRESSION; HSNF5/INI1; GENE; INI1/SMARCB1;
D O I
10.3760/cma.j.issn.0366-6999.2012.03.023
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Integrase interactor 1 (INI1), which encodes a component of the ATP-dependent chromatin remodeling hSWI-SNF complex, has been identified as a tumor suppressor in many tumors. Nonetheless, the role of INI1 in gastric tumor progression is not known exactly. The aim of this research was to investigate the effect of INI1 in the carcinogenesis and progression of gastric cancer. Methods Gastric tumor tissues with different differentiation levels from clinical gastric carcinoma samples and adjacent control normal tissues were taken. Expression levels of INI1 were detected by quantitative reverse transcriptation-polymerase chain reaction (RT-PCR) and Western blotting. Gastric cancer cell line SGC7901 was transfected with INI1 eukaryotic expressing vector INI1-GFP. Cell proliferation activities were assessed by MTT; cell count and cell cycle were detected by flow cytometry (FCM); cell apoptosis were measured by TUNEL and FCM; cell migration and invasiveness were evaluated by wound healing and transwell assays. Expression levels of INI1 and proliferation-related genes including p16, p21, cyclin D1 and cyclin A, apoptosis genes p53, B-cell non-Hodgkin lymphoma-2 (Bcl-2), Bcl-2-associated x protein (Bax) and caspase-3, and invasion-related genes including intercellular adhesion molecule 1 (ICAM1), matrix metalloproteinase 2 (MMP2), MMP9 and tissue inhibitor of matrix metalloproteinase 1 (TIMP1), were detected by quantitative RT-PCR and Western blotting. Results INI1 expression levels were lower in gastric carcinoma compared with adjacent control normal tissues. Overexpression of INI1 in SGC7901 cells inhibited its proliferation and invasiveness, but increased anoikis and G(0)/G(1) cell number. INI1-GFP transfection upregulated expression of INI1 and proliferation related genes p16 and p21, apoptosis genes p53 and Bax, and invasion-related genes TIMP1; cyclin D1, cyclin A, Bcl2, ICAM1, MMP2 and MMP9 were downregulated, and there was no significant change in caspase 3 levels. Conclusion INI1 plays a key role in gastric carcinogenesis by affecting proliferation, apoptosis and invasion. Chin Med J 2012;125(3):527-532
引用
收藏
页码:527 / 532
页数:6
相关论文
共 31 条
  • [11] Cancer statistics, 2002
    Jemal, A
    Thomas, A
    Murray, T
    Thun, M
    [J]. CA-A CANCER JOURNAL FOR CLINICIANS, 2002, 52 (01) : 23 - 47
  • [12] Patterns of cancer incidence, mortality, and prevalence across five continents: Defining priorities to reduce cancer disparities in different geographic regions of the world
    Kamangar, Farin
    Dores, Graca M.
    Anderson, William F.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (14) : 2137 - 2150
  • [13] Knock down of hSNF5/Ini1 causes cell cycle arrest and apoptosis in a p53-dependent manner
    Kato, Hiroyuki
    Honma, Reiko
    Sanda, Takaomi
    Fujiwara, Toshiyoshi
    Ito, Emi
    Yanagisawa, Yuka
    Imai, Jun-ichi
    Okamoto, Takashi
    Watanabe, Shinya
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 361 (03) : 580 - 585
  • [14] SMARCB1/INI1 protein expression in round cell soft tissue sarcomas associated with chromosomal translocations involving EWS:: A special reference to SMARCB1/INI1 negative variant extraskeletal myxoid chondrosarcoma
    Kohashi, Kenichi
    Oda, Yoshinao
    Yamamoto, Hidetaka
    Tamiya, Sadafumi
    Oshiro, Yumi
    Izumi, Teiyu
    Taguchi, Tomoaki
    Tsuneyoshi, Masazumi
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2008, 32 (08) : 1168 - 1174
  • [15] Highly aggressive behavior of malignant rhabdoid tumor:: a special reference to SMARCB1/INI1 gene alterations using molecular genetic analysis including quantitative real-time PCR
    Kohashi, Kenichi
    Oda, Yoshinao
    Yamamoto, Hidetaka
    Tamiya, Sadafumi
    Izumi, Teiyu
    Ohta, Shigeru
    Taguchi, Tomoaki
    Suita, Sachiyo
    Tsuneyoshi, Masazumi
    [J]. JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2007, 133 (11) : 817 - 824
  • [16] Reduced expression of SMARCB1/INI1 protein in synovial sarcoma
    Kohashi, Kenichi
    Oda, Yoshinao
    Yamamoto, Hidetaka
    Tamiya, Sadafumi
    Matono, Hiroshi
    Iwamoto, Yukihide
    Taguchi, Tomoaki
    Tsuneyoshi, Masazumi
    [J]. MODERN PATHOLOGY, 2010, 23 (07) : 981 - 990
  • [17] Infrequent SMARCB1/INI1 gene alteration in epithelioid sarcoma: a useful tool in distinguishing epithelioid sarcoma from malignant rhabdoid tumor
    Kohashi, Kenichi
    Izumi, Teiyu
    Oda, Yoshinao
    Yamamoto, Hidetaka
    Tamiya, Sadafumi
    Taguchi, Tomoaki
    Iwamoto, Yukihide
    Hasegawa, Tadashi
    Tsuneyoshi, Masazumi
    [J]. HUMAN PATHOLOGY, 2009, 40 (03) : 349 - 355
  • [18] Loss of the epigenetic tumor suppressor SNF5 leads to cancer without genomic instability
    McKenna, Elizabeth S.
    Sansam, Courtney G.
    Cho, Yoon-Jae
    Greulich, Heidi
    Evans, Julia A.
    Thom, Christopher S.
    Moreau, Lisa A.
    Biegel, Jaclyn A.
    Pomeroy, Scott L.
    Roberts, Charles W. M.
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (20) : 6223 - 6233
  • [19] The tumor suppressor hSNF5/INI1 modulates cell growth and actin cytoskeleton organization
    Medjkane, S
    Novikov, E
    Versteege, I
    Delattre, O
    [J]. CANCER RESEARCH, 2004, 64 (10) : 3406 - 3413
  • [20] Extrarenal rhabdoid tumors of soft tissue: Clinicopathological and molecular genetic review and distinction from other soft-tissue sarcomas with rhabdoid features
    Oda, Yoshinao
    Tsuneyoshi, Masazumi
    [J]. PATHOLOGY INTERNATIONAL, 2006, 56 (06) : 287 - 295