Expressions of stemness markers in keloid tissue

  • Sri S. Ningsih Master of Biomedical Sciences, Faculty of Medicine, University of Indonesia, Jakarta
  • Dewi H. Sari Master of Biomedical Sciences, Faculty of Medicine, University of Indonesia, Jakarta
  • Radiana D. Antarianto Department of Histology, Faculty of Medicine, Universitas Indonesia, Jakarta
  • Novi S. Hardiany Department of Biochemistry and Molecular Biology, Center of Hypoxia and Oxidative Stress Studies, Faculty of Medicine, Universitas Indonesia, Jakarta
  • Mohamad Sadikin Department of Biochemistry and Molecular Biology, Center of Hypoxia and Oxidative Stress Studies, Faculty of Medicine, Universitas Indonesia, Jakarta
  • Septelia I. Wanandi Department of Biochemistry and Molecular Biology, Center of Hypoxia and Oxidative Stress Studies, Faculty of Medicine, Universitas Indonesia, Jakarta
  • Sri W.A. Jusman Department of Biochemistry and Molecular Biology, Center of Hypoxia and Oxidative Stress Studies, Faculty of Medicine, Universitas Indonesia, Jakarta
Keywords: ALDH1, keloid, Oct-4, stemness
Abstract viewed: 1018 times
PDF downloaded: 696 times
HTML downloaded: 102 times
EPUB downloaded: 119 times

Abstract

Background: Keloid is an abnormal wound healing process that extends beyond the site of injury. Keloid and tumor’s shared similarity of recurrence suggesting a shared underlying mechanism that involves stemness. Octamer-binding transcription factor-4 (Oct-4) and aldehyde dehydrogenase-1 (ALDH1) are stem cell stemness markers. This study aimed to analyze Oct-4 and ALDH1 expressions in keloid tissues.

Methods: Samples were obtained from keloid tissue excisions from three keloid patients and post-circumcision preputial skin from three healthy donors (normal control) in accordance with the local ethical committee regulation. Total RNA was isolated using TriPure Isolation kit (Ameritech), and expressions of Oct4 and ALDH1 mRNA in keloid and preputial skin were determined by quantitative reverse transcription–polymerase chain reaction (qRT-PCR) using Livak method.

Results: The qRT-PCR analysis revealed the expressions of Oct4 and ALDH1 in keloid and preputial skin tissues. Keloid tissues exhibited lower expression levels of Oct-4 and ALDH1 than the preputial skin. The difference was statistically insignificant.

Conclusion: Keloid tissues express Oct-4 and ALDH1 as stemness markers, and the stemness characteristics of keloid might be similar to a normal skin.

References

  1. Goder M, Kornhaber R, Bordoni D, Winkler E, Haik J, Tessone A. Cutaneous basal cell carcinoma arising within a keloid scar: a case report. Onco Targets Ther. 2016;9:4793-6. https://doi.org/10.2147/OTT.S113724

  2. Ma X, Chen J, Xu B, Long X, Qin H, Zhao RC, et al. Keloid-derived keratinocytes acquire a fibroblast-like appearance and an enhanced invasive capacity in a hypoxic microenvironment in vitro. Int J Mol Med. 2015;35(5):1246-56. https://doi.org/10.3892/ijmm.2015.2135

  3. Zhang Q, Yidi W, Ann DK, Messadi DV, Tuan T, Kelly AP, et al. Mechanisms of hypoxic regulation of plasminogen activator inhibitor-1 gene expression in keloid fibroblasts. J Invest Dermatol. 2003;121(5):1005-12. https://doi.org/10.1046/j.1523-1747.2003.12564.x

  4. Zeineddine D, Hammoud AA, Mortada M, Boeuf H. The Oct4 protein: more than a magic stemness marker. Am J Stem Cells. 2014;3(2):74-82.

  5. Samardzija C, Michael Q, Jock KF, Nuzhat A. Attributes of Oct4 in stem cell biology: perspectives on cancer stem cells of the ovary. J Ovarian Res. 201-42. https://doi.org/10.1186/1757-2215-5-37

  6. Deng C, Wang B, Zhang Z, Sun G, Zhu J, Wang D, et al. The expressions of notch genes in human keloid-derived mesenchymal-like stem cells. Zhonghua Zheng Xing Wai Ke Za Zhi. 2014;30(3):197-202.

  7. Grant C, Chudakova DA, Itinteang T, Chibnall AM, Brasch HD, Davis PF, et al. Expression of embryonic stem cell markers in keloid-associated lymphoid tissue. J Clin Pathol. 2016;69(7):643-6. https://doi.org/10.1136/jclinpath-2015-203483

  8. Douville J, Beaulieu R, Balicki D. ALDH1 as a functional marker of cancer stem and progenitor cells. Stem Cells Dev. 2009;18(1):17-26. https://doi.org/10.1089/scd.2008.0055

  9. Lohberger B, Beate R, Nicole S, Markus A, Bernadette LA, Sonja MW, et al. Aldehyde dehydrogenase 1, a potential marker for cancer stem cells in human sarcoma. PLoS One. 2012;7(8):1-10. https://doi.org/10.1371/journal.pone.0043664

  10. Hahn JM, Glaser K, McFarland KL, Aronow BJ, Boyce ST, Supp DM. Keloid-derived keratinocytes exhibit an abnormal gene expression profile consistent with a distinct causal role in keloid pathology. Wound Repair Regen. 2013;21(4):530-44. https://doi.org/10.1111/wrr.12060

  11. Battula VL, Evans KW, Hollier BG, Shi Y, Marini FC, Ayyanan A, et al. Epithelial-mesenchymal transition-derived cells exhibit multilineage differentiation potential similar to mesenchymal stem cells. Stem Cells. 2010;28(8):1435-45. https://doi.org/10.1002/stem.467

  12. Samardzija C, Quinn M, Findlay JK, Ahmed N. Attributes of Oct4 in stem cell biology: perspectives on cancer stem cells of the ovary. J Ovarian Res. 2012;5(37):1-12. https://doi.org/10.1186/1757-2215-5-37

  13. Nakahata K, Shuichiro U, Shimpei N, Miyoko K, Masahiro Z, Takaharu O, et al. Aldehyde dehydrogenase 1 (ALDH1) is a potential marker for cancer stem cells in embryonal rhabdomyosarcoma. PLoS One. 2015;10(4):1-16. https://doi.org/10.1371/journal.pone.0125454

  14. Jumper N, Hodgkinson T, Paus R, Bayat A. Site-specific gene expression profiling as a novel strategy for unravelling keloid disease pathobiology. PLoS One. 2017;12(3):1-33. https://doi.org/10.1371/journal.pone.0172955

  15. Yan L, Rui C, Yuan BL, Lian ZW, Bo P, Xiao YL, et al. MiR-21-5p links epithelial-mMesenchymal transition phenotype with stem-like cell signatures via AKT signaling in keloid keratinocytes. Sci Rep. 2016;6:28281. https://doi.org/10.1038/srep28281

  16. Wang DL, Zhu JJ, Deng CL, Wang B, Yu LM. Identification of biological characteristics of human keloid-derived stem cells. Zhonghua Shao Shang Za Zhi. 2011;27(3):210-4.

  17. Rodemann HP, Rennekampff HO. Functional diversity of fibroblast. In: Mueller MM, Fusenig NE editors. Tumor-associated fibroblast and their matrix. New York: Springer; 2014. P.23-36.

  18. Chipev, Simman R, Hatch G, Katz AE, Siegel DM, Simon M. Myofibroblast phenotype and apoptosis in keloid and palmar fibroblasts invitro. Cell Death Differ. 2000;7:166-76. https://doi.org/10.1038/sj.cdd.4400605

  19. Wulandari E, Jusman SW, Moenadjat Y, Jusuf AA, Sadikin M. Expressions of collagen I and III in hypoxic keloid tissue. Kobe J Med Sci. 2016;62(3):E58-69.

Published
2018-10-12
How to Cite
1.
Ningsih SS, Sari DH, Antarianto RD, Hardiany NS, Sadikin M, Wanandi SI, Jusman SW. Expressions of stemness markers in keloid tissue. Med J Indones [Internet]. 2018Oct.12 [cited 2024Apr.27];27(3):145-9. Available from: http://mji.ui.ac.id/journal/index.php/mji/article/view/1920
Section
Basic Medical Research