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Molecular Biology Reports

, Volume 46, Issue 1, pp 77–82 | Cite as

ARA lncRNA, is upregulated in liver and breast tumor tissues

  • Farzaneh Raeisi
  • Mahdieh Abolfathi
  • Raheleh Ahmadi-Naji
  • Sara Iranparast
  • Esmat Noshadi
  • Arvand Akbari
  • Esmaeil Mahmoudi
  • Mansoor Khaledi
  • Asghar ArshiEmail author
Original Article
  • 144 Downloads

Abstract

Important regulatory roles of long non-coding RNAs (lncRNAs) have been recently found, and reported as useful biomarkers in cancer. To identify a potential expression of the new discovered lncRNA (ARA), during promotes cell proliferation, apoptosis inhibit, migration and cell cycle arrest, we firstly evaluate its expression in two cancer tissues (breast cancer and liver cancer) and then compared its variability expression in tumor versus non-tumor samples. Expression profile of ARA lncRNA was evaluated using qRT-PCR in paired tumor and marginal non-tumor samples collected from patients who had been referred to the Shiraz General. After RNA extraction from tissue samples, cDNA synthesis and RT-qPCR method were performed according to the protocols. ARA lncRNA expression level was calculated using 2−ΔΔCt method. Principal-component analysis followed by receiver operating characteristic curve analyses was performed to evaluate the diagnostic potential of selected lncRNA. Our data revealed a significant upregulation (P < 0.001) of ARA in breast and liver tumor tissues, in comparison to same patients non-tumor marginal samples. Also, there was a significant difference between the expression of ARA lncRNA in breast cancer and liver cancer patients (P < 0.05). In conclusion, the results of our study suggest a possible role of ARA lncRNA in proliferation of breast and liver tissues, as well as its potential usefulness as a novel diagnostic biomarker for breast and liver tumors.

Keywords

LncRNA ARA Breast cancer Liver cancer 

Notes

Acknowledgements

The authors are grateful to the staffs of research deputy of Shahrekord University of Medial Sciences and Cellular and Molecular Research Center, Shahrekord University of Medical Sciences.

Author contributions

FR, MA, EM and SI; literature review, manuscript writing and data collection. AA; literature review and manuscript revision, EN, AA; manuscript revision and RA-N, MK; literature review.

Compliance with ethical standards

Conflict of interest

The authors declare they have no conflict of interest.

Ethical approval

All applicable international, national, and institutional guidelines for the care of human were followed.

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Copyright information

© Springer Nature B.V. 2018

Authors and Affiliations

  1. 1.Young Researchers and Elite Club, Shahrekord BranchIslamic Azad UniversityShahrekordIran
  2. 2.Department of Immunology, Basic Health Sciences InstituteShahrekord University of Medical SciencesShahrekordIran
  3. 3.Student Research CommitteeShahrekord University of Medical SciencesShahrekordIran
  4. 4.Department of ImmunologyAhvaz University of Medical SciencesAhvazIran
  5. 5.Department of Biology, Faculty of Science, Fars Science and Research BranchIslamic Azad UniversityMarvdashtIran
  6. 6.Department of Biology, Faculty of Science, Marvdasht BranchIslamic Azad UniversityMarvdashtIran
  7. 7.Medical Microbiology, Student Research CommitteeShahrekord University of Medical SciencesShahrekordIran
  8. 8.Young Researchers and Elite Club, Najafabad BranchIslamic Azad UniversityNajafabadIran

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