Literature DB >> 27565813

Expression of the circulating and the tissue microRNAs after surgery, chemotherapy, and radiotherapy in mice mammary tumor.

Sadaf Farsinejad1, Mahdi Rahaie1, Ali Mohammad Alizadeh2, Mohammad Mir-Derikvand1, Zohre Gheisary1, Hassan Nosrati3, Solmaz Khalighfard4.   

Abstract

The expression of microRNAs (miRNAs), as novel biomarkers, is subject to change in many cancers. Therefore, the overall profile of miRNAs can be used for detection of cancer type, response to therapies, pathological variables, and other factors related to the disease. In this study, to evaluate miRNA expression associated with the tumor progression and response to treatment, 60 BALB/c mice received subcutaneous injections of 4T1 cells. The study includes ten groups: one group as control, six groups were euthanized at different time points to assess the role of miRNA expression in the tumor progression, and three groups received chemotherapy, radiotherapy, and surgery to evaluate miRNA expression in response to treatment. MicroRNAs were extracted from the breast tumor and the plasma samples, and their relative expressions were quantified using qRT-PCR. MiR-155 expression was increased in the plasma in the early weeks after the cell injection but decreased in the plasma after surgery and radiotherapy and also in tumor samples after chemotherapy and radiotherapy. MiR-10b expression was increased in the late weeks both in the plasma and the tumor and was decreased in the plasma after radiotherapy and surgery and in the tumor after radiotherapy. MiR-21 expression was increased in the plasma and the tumor tissue during the disease progression at the third and the fourth weeks following tumor induction but was decreased in the plasma in all the therapy groups. Interestingly, miR-125a showed a significant decrease during the tumor progression, and its expression was increased after the treatment. Our results showed that the candidate miRNAs could be divided into two groups of oncomiRs and tumor suppressor miR based on their deregulation after tumor growth and treatments. It seems that the oncomiRs in the plasma can be an ideal noninvasive candidate biomarker for the early detection of breast cancer and also for following the response of the common therapies.

Entities:  

Keywords:  Breast cancer; Chemotherapy; Mice; MicroRNA; Radiotherapy; Surgery

Mesh:

Substances:

Year:  2016        PMID: 27565813     DOI: 10.1007/s13277-016-5292-7

Source DB:  PubMed          Journal:  Tumour Biol        ISSN: 1010-4283


  54 in total

1.  Coordinate suppression of ERBB2 and ERBB3 by enforced expression of micro-RNA miR-125a or miR-125b.

Authors:  Gary K Scott; Andrei Goga; Dipa Bhaumik; Crystal E Berger; Christopher S Sullivan; Christopher C Benz
Journal:  J Biol Chem       Date:  2006-11-16       Impact factor: 5.157

2.  MicroRNA expression after ionizing radiation in human endothelial cells.

Authors:  Mechthild Wagner-Ecker; Christian Schwager; Ute Wirkner; Amir Abdollahi; Peter E Huber
Journal:  Radiat Oncol       Date:  2010-03-26       Impact factor: 3.481

3.  MicroRNA-206, let-7a and microRNA-21 pathways involved in the anti-angiogenesis effects of the interval exercise training and hormone therapy in breast cancer.

Authors:  Amin Isanejad; Ali Mohammad Alizadeh; Sadegh Amani Shalamzari; Hamid Khodayari; Saeed Khodayari; Vahid Khori; Najmeh Khojastehnjad
Journal:  Life Sci       Date:  2016-02-26       Impact factor: 5.037

Review 4.  Cell-free nucleic acids as biomarkers in cancer patients.

Authors:  Heidi Schwarzenbach; Dave S B Hoon; Klaus Pantel
Journal:  Nat Rev Cancer       Date:  2011-05-12       Impact factor: 60.716

5.  Pre-B cell proliferation and lymphoblastic leukemia/high-grade lymphoma in E(mu)-miR155 transgenic mice.

Authors:  Stefan Costinean; Nicola Zanesi; Yuri Pekarsky; Esmerina Tili; Stefano Volinia; Nyla Heerema; Carlo M Croce
Journal:  Proc Natl Acad Sci U S A       Date:  2006-04-25       Impact factor: 11.205

6.  Clinical significance of serum miR-21 in breast cancer compared with CA153 and CEA.

Authors:  Jianjian Gao; Qingyun Zhang; Jianjun Xu; Lijuan Guo; Xuefeng Li
Journal:  Chin J Cancer Res       Date:  2013-12       Impact factor: 5.087

7.  Programmed cell death 4 (PDCD4) is an important functional target of the microRNA miR-21 in breast cancer cells.

Authors:  Lisa B Frankel; Nanna R Christoffersen; Anders Jacobsen; Morten Lindow; Anders Krogh; Anders H Lund
Journal:  J Biol Chem       Date:  2007-11-08       Impact factor: 5.157

8.  MicroRNA-21 targets the tumor suppressor gene tropomyosin 1 (TPM1).

Authors:  Shuomin Zhu; Min-Liang Si; Hailong Wu; Yin-Yuan Mo
Journal:  J Biol Chem       Date:  2007-03-15       Impact factor: 5.157

Review 9.  Mechanisms of resistance to endocrine therapy in breast cancer: focus on signaling pathways, miRNAs and genetically based resistance.

Authors:  Rocío García-Becerra; Nancy Santos; Lorenza Díaz; Javier Camacho
Journal:  Int J Mol Sci       Date:  2012-12-20       Impact factor: 5.923

Review 10.  Radiotherapy in the management of early breast cancer.

Authors:  Wei Wang
Journal:  J Med Radiat Sci       Date:  2013-02-03
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  5 in total

Review 1.  The fundamental role of miR-10b in metastatic cancer.

Authors:  Patrick Sheedy; Zdravka Medarova
Journal:  Am J Cancer Res       Date:  2018-09-01       Impact factor: 6.166

2.  Effects of Lactobacillus acidophilus and Bifidobacterium bifidum Probiotics on the Expression of MicroRNAs 135b, 26b, 18a and 155, and Their Involving Genes in Mice Colon Cancer.

Authors:  Zahra Heydari; Mahdi Rahaie; Ali Mohammad Alizadeh; Shahram Agah; Solmaz Khalighfard; Sahar Bahmani
Journal:  Probiotics Antimicrob Proteins       Date:  2019-12       Impact factor: 4.609

3.  Response to neoadjuvant chemotherapy in breast cancer: do microRNAs matter?

Authors:  Dinara Ryspayeva; Volodymyr Halytskiy; Nazarii Kobyliak; Iryna Dosenko; Artem Fedosov; Mariia Inomistova; Tetyana Drevytska; Vitalyi Gurianov; Oksana Sulaieva
Journal:  Discov Oncol       Date:  2022-06-07

4.  Plasma miR-21, miR-155, miR-10b, and Let-7a as the potential biomarkers for the monitoring of breast cancer patients.

Authors:  Solmaz Khalighfard; Ali Mohammad Alizadeh; Shiva Irani; Ramesh Omranipour
Journal:  Sci Rep       Date:  2018-12-19       Impact factor: 4.379

5.  MicroRNA-155, induced by FOXP3 through transcriptional repression of BRCA1, is associated with tumor initiation in human breast cancer.

Authors:  Song Gao; Yicun Wang; Meng Wang; Zhi Li; Zhiying Zhao; Raymond X Wang; Rong Wu; Zhengwei Yuan; Ranji Cui; Kai Jiao; Lizhong Wang; Ling Ouyang; Runhua Liu
Journal:  Oncotarget       Date:  2017-06-20
  5 in total

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