Expression levels of genes involved in cell adhesion and motility correlate with poor clinicopathological features of epithelial ovarian cancer

被引:1
作者
Boljevic, Ivana [1 ]
Malisic, Emina [1 ]
Milovic-Kovacevic, Marjana [2 ]
Jovanic, Irena [3 ]
Jankovic, Radmila [1 ]
机构
[1] Inst Oncol & Radiol Serbia, Dept Expt Oncol, Pasterova 14, Belgrade, Serbia
[2] Inst Oncol & Radiol Serbia, Dept Med Oncol, Pasterova 14, Belgrade, Serbia
[3] Inst Oncol & Radiol Serbia, Dept Pathol, Pasterova 14, Belgrade, Serbia
来源
JOURNAL OF BUON | 2020年 / 25卷 / 04期
关键词
CALD1; epithelial ovarian cancer; epithelial mesenchymal transition; ITGAV; V INTEGRIN EXPRESSION; ACTIN CYTOSKELETON; CALDESMON; METASTASIS; MIGRATION; INVASION; OVEREXPRESSION; RECURRENCE; PROGNOSIS; EMT;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Changes in the expression levels of genes involved in cancer cell adhesion and motility have been reported to have an important role in tumor progression. In this study, we aimed to investigate the clinical significance of ITGAV and CALD1 gene expression in epithelial ovarian cancer (EOC), the most lethal gynecological malignancy. Methods: Reverse transcription quantitative polymerase chain reaction was used to evaluate ITGAV and CALD1 expression levels in 47 EOC and 19 benign formalin-fixed paraffin-embedded samples. We used Spearman's test to determine the association between ITGAV and CALD1 expression and Wilcoxon test to compare expression levels between malignant and benign ovarian tumor specimens as well as to determine their association with clinicopathological characteristics of EOC. Survival analysis was done by the Kaplan Meier method and the log-rank test. P <= 0.05 was considered statistically significant. Results: CALD1 and ITGAV showed significantly lower expression in EOC than in benign ovarian samples (p<0.001). Furthermore, CALD1 was significantly lower expressed in high-grade tumors (p=0.037) while there was a trend for a lower expression of ITGAV in tumors with high histological grade (p=0.043), in tumors with ascites (p=0.055), and in tumors of patients who relapsed (p=0.083). We also found a significant positive association between ITGAV and CALD1 expression (rho=0.640, p<0.001) in EOC samples. Kaplan Meier analysis showed no significant impact of ITGAV and CALD1 expression levels on overall survival of EOC patients (p=0.149 and p=0.430, respectively). Conclusion: Our findings indicate that CALD1 and ITGAV gene expression levels correlate with poor clinicopathological features of the EOC.
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页码:1911 / 1917
页数:7
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共 41 条
  • [1] Intraperitoneal cisplatin and paclitaxel in ovarian cancer
    Armstrong, DK
    Bundy, B
    Wenzel, L
    Huang, HQ
    Baergen, R
    Lele, S
    Copeland, LJ
    Walker, JL
    Burger, RA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (01) : 34 - 43
  • [2] Epithelial-mesenchymal transition in lung development and disease: does it exist and is it important?
    Bartis, Domokos
    Mise, Nikica
    Mahida, Rahul Y.
    Eickelberg, Oliver
    Thickett, David R.
    [J]. THORAX, 2014, 69 (08) : 760 - 765
  • [3] Integrins in the Spotlight of Cancer
    Bianconi, Daniela
    Unseld, Matthias
    Prager, Gerald W.
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (12)
  • [4] Overexpression of Caldesmon Is Associated With Lymph Node Metastasis and Poorer Prognosis in Patients With Oral Cavity Squamous Cell Carcinoma
    Chang, Kai-Ping
    Wang, Chih-Lueh Albert
    Kao, Huang-Kai
    Liang, Ying
    Liu, Shiau-Chin
    Huang, Ling-Ling
    Hseuh, Chuen
    Hsieh, Ya-Ju
    Chien, Kun-Yi
    Chang, Yu-Sun
    Yu, Jau-Song
    Chi, Lang-Ming
    [J]. CANCER, 2013, 119 (22) : 4003 - 4011
  • [5] Chen LY, 2018, J BUON, V23, P428
  • [6] CNTO 95, a fully human anti αv integrin antibody, inhibits cell signaling, migration, invasion, and spontaneous metastasis of human breast cancer cells
    Chen, Qiming
    Manning, Carol D.
    Millar, Hillary
    McCabe, Francis L.
    Ferrante, Catherine
    Sharp, Celia
    Shahied-Arruda, Lillian
    Doshi, Parul
    Nakada, Marian T.
    Anderson, G. Mark
    [J]. CLINICAL & EXPERIMENTAL METASTASIS, 2008, 25 (02) : 139 - 148
  • [7] Extracellular matrix expression in metastasizing and nonmetastasizing adenocarcinomas of the lung
    Clarke, MR
    Landreneau, RJ
    Finkelstein, SD
    Wu, TT
    Ohori, P
    Yousem, SA
    [J]. HUMAN PATHOLOGY, 1997, 28 (01) : 54 - 59
  • [8] Expression of integrin genes and proteins in progression and dissemination of colorectal adenocarcinoma
    Denadai, Marcos V. A.
    Viana, Luciano S.
    Affonso, Renato J., Jr.
    Silva, Sandra R.
    Oliveira, Indhira D.
    Toledo, Silvia R.
    Matos, Delcio
    [J]. BMC CLINICAL PATHOLOGY, 2013, 13
  • [9] Targeting epithelial-mesenchymal transition and cancer stem cells for chemoresistant ovarian cancer
    Deng, Junli
    Wang, Li
    Chen, Hongmin
    Hao, Jingli
    Ni, Jie
    Chang, Lei
    Duan, Wei
    Graham, Peter
    Li, Yong
    [J]. ONCOTARGET, 2016, 7 (34) : 55771 - 55788
  • [10] A novel role for junctional adhesion molecule-A in tumor proliferation: Modulation by an anti-JAM-A monoclonal antibody
    Goetsch, Liliane
    Haeuw, Jean-Francois
    Beau-Larvor, Charlotte
    Gonzalez, Alexandra
    Zanna, Laurence
    Malissard, Martine
    Lepecquet, Anne-Marie
    Robert, Alain
    Bailly, Christian
    Broussas, Matthieu
    Corvaia, Nathalie
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2013, 132 (06) : 1463 - 1474