Down-regulation of miRNA-148a and miRNA-625-3p in colorectal cancer is associated with tumor budding

被引:44
作者
Baltruskeviciene, Edita [1 ]
Schveigert, Diana [2 ]
Stankevicius, Vaidotas [2 ,3 ]
Mickys, Ugnius [4 ]
Zvirblis, Tadas [5 ]
Bublevic, Jaroslav [1 ]
Suziedelis, Kestutis [2 ,6 ]
Aleknavicius, Eduardas [1 ,7 ]
机构
[1] Natl Canc Inst, Dept Med Oncol, Santariskiu 1, LT-08660 Vilnius, Lithuania
[2] Natl Canc Inst, Mol Oncol Lab, Vilnius, Lithuania
[3] Vilnius Univ, Inst Biotechnol, Life Sci Ctr, Vilnius, Lithuania
[4] Affiliate Vilnius Univ Hosp Santaros Klin, Natl Ctr Pathol, Vilnius, Lithuania
[5] Vilnius Univ Hosp Santaros Klin, Hematol Oncol & Transfusiol Ctr, Vilnius, Lithuania
[6] Vilnius Univ, Inst Biosci, Life Sci Ctr, Vilnius, Lithuania
[7] Vilnius Univ, Dept Radiol Nucl Med & Phys Med, Fac Med, Vilnius, Lithuania
关键词
MiRNA-148a; miRNA-625-3p; microRNA; Tumor budding; Colorectal cancer; Oxaliplatin; EPITHELIAL-MESENCHYMAL TRANSITION; POOR-PROGNOSIS; DECREASED EXPRESSION; TARGET INTERACTIONS; GASTRIC-CANCER; CELL INVASION; MICRORNA-148A; MIR-148A; METASTASIS; CHEMOTHERAPY;
D O I
10.1186/s12885-017-3575-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: MiRNAs are often deregulated in colorectal cancer and might function as tumor suppressors or as oncogenes. They participate in controlling key signaling pathways involved in proliferation, invasion and apoptosis and may serve as prognostic and predictive markers. In this study we aimed to evaluate the role of miRNA-148a and miRNA-625-3p in metastatic colorectal cancer. Methods: Fifty-four patients with a first-time diagnosed CRC receiving FOLFOX +/- Bevacizumab were involved in the study. Tumor samples underwent routine pathology examination including evaluation for tumor budding and KRAS. MiRNA-148a and miRNA-625-3p expression analysis was done by RT-PCR. Associations between expression of both miRNAs and clinico-pathological factors, treatment outcomes and survival were analyzed. Results: Both miRNA-148a and miRNA-625-3p were down-regulated in the tumors compared to normal colonic mucosa. Significantly lower expression of both miRNAs was noticed in tumors with budding phenomenon compared to tumors without it (median values of miRNA-148a were 0.314 and 0.753 respectively, p = 0.011, and 0.404 and 0.620 respectively for miRNA-625-3p, p = 0.036). Significantly lower expression of miRNA-625-3p was detected in rectal tumors, compared to tumors in the colon (median 0.390 and 0.665 respectively, p = 0.037). Progression free survival was significantly lower in patients with high miRNA-148a expression (6 and 9 months respectively, p = 0.033), but there were no significant differences in PFS for miRNA-625-3p and in overall survival for both miRNAs. Conclusions: There was a significant relationship between low miRNA-148a and miRNA-625-3p expression and tumor budding, which is thought to represent epithelial-mesenchymal transition. Both studied miRNAs may be associated with a more aggressive phenotype and could be the potential prognostic and predictive biomarkers in CRC. Further investigation is needed to confirm miRNAs involvement in EMT, and their prognostic and predictive value.
引用
收藏
页数:10
相关论文
共 50 条
  • [1] [Anonymous], 2018, ANTI-CANCER DRUG, DOI [DOI 10.3322/caac.20115, DOI 10.1097/CAD.0000000000000617]
  • [2] Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues
    Bandres, E.
    Cubedo, E.
    Agirre, X.
    Malumbres, R.
    Zarate, R.
    Ramirez, N.
    Abajo, A.
    Navarro, A.
    Moreno, I.
    Monzo, M.
    Garcia-Foncillas, J.
    [J]. MOLECULAR CANCER, 2006, 5 (1)
  • [3] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29
  • [4] Cancer cell invasion and EMT marker expression: a three-dimensional study of the human cancer-host interface
    Bronsert, P.
    Enderle-Ammour, K.
    Bader, M.
    Timme, S.
    Kuehs, M.
    Csanadi, A.
    Kayser, G.
    Kohler, I.
    Bausch, D.
    Hoeppner, J.
    Hopt, U. T.
    Keck, T.
    Stickeler, E.
    Passlick, B.
    Schilling, O.
    Reiss, C. P.
    Vashist, Y.
    Brabletz, T.
    Berger, J.
    Lotz, J.
    Olesch, J.
    Werner, M.
    Wellner, U. F.
    [J]. JOURNAL OF PATHOLOGY, 2014, 234 (03) : 410 - 422
  • [5] The MicroRNA-148/152 Family: Multi-faceted Players
    Chen, Yue
    Song, Yong-Xi
    Wang, Zhen-Ning
    [J]. MOLECULAR CANCER, 2013, 12
  • [6] Altered Expression of MiR-148a and MiR-152 in Gastrointestinal Cancers and Its Clinical Significance
    Chen, Yue
    Song, Yongxi
    Wang, Zhenning
    Yue, Zhenyu
    Xu, Huimian
    Xing, Chengzhong
    Liu, Zhuangkai
    [J]. JOURNAL OF GASTROINTESTINAL SURGERY, 2010, 14 (07) : 1170 - 1179
  • [7] miRTarBase 2016: updates to the experimentally validated miRNA-target interactions database
    Chou, Chih-Hung
    Chang, Nai-Wen
    Shrestha, Sirjana
    Hsu, Sheng-Da
    Lin, Yu-Ling
    Lee, Wei-Hsiang
    Yang, Chi-Dung
    Hong, Hsiao-Chin
    Wei, Ting-Yen
    Tu, Siang-Jyun
    Tsai, Tzi-Ren
    Ho, Shu-Yi
    Jian, Ting-Yan
    Wu, Hsin-Yi
    Chen, Pin-Rong
    Lin, Nai-Chieh
    Huang, Hsin-Tzu
    Yang, Tzu-Ling
    Pai, Chung-Yuan
    Tai, Chun-San
    Chen, Wen-Liang
    Huang, Chia-Yen
    Liu, Chun-Chi
    Weng, Shun-Long
    Liao, Kuang-Wen
    Hsu, Wen-Lian
    Huang, Hsien-Da
    [J]. NUCLEIC ACIDS RESEARCH, 2016, 44 (D1) : D239 - D247
  • [8] Molecular and pathogenetic aspects of tumor budding in colorectal cancer
    Dawson, Heather
    Lugli, Alessandro
    [J]. FRONTIERS IN MEDICINE, 2015, 2 : 11
  • [9] Tumour budding in colorectal cancer: what do we know and what can we do?
    De Smedt, Linde
    Palmans, Sofie
    Sagaert, Xavier
    [J]. VIRCHOWS ARCHIV, 2016, 468 (04) : 397 - 408
  • [10] Tumor Budding in Colorectal Carcinoma Confirmation of Prognostic Significance and Histologic Cutoff in a Population-based Cohort
    Graham, Rondell P.
    Vierkant, Robert A.
    Tillmans, Lori S.
    Wang, Alice H.
    Laird, Peter W.
    Weisenberger, Daniel J.
    Lynch, Charles F.
    French, Amy J.
    Slager, Susan L.
    Raissian, Yassaman
    Garcia, Joaquin J.
    Kerr, Sarah E.
    Lee, Hee Eun
    Thibodeau, Stephen N.
    Cerhan, James R.
    Limburg, Paul J.
    Smyrk, Thomas C.
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2015, 39 (10) : 1340 - 1346