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2018 | 23 |

Tytuł artykułu

The diagnostic value and pathogenetic role of lncRNA-ATB in patients with osteoarthritis

Autorzy

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Background: In view of the roles of long non-coding RNAs (lncRNAs) in human diseases and the high incidence of osteoarthritis, we investigated the role of long non-coding RNA activated by transforming growth factor-β (lncRNA-ATB) in osteoarthritis and explored its diagnostic value for this disease. Methods: The study involved 98 patients with osteoarthritis and 76 healthy subjects. Blood was extracted from each participant and the expression of lncRNA-ATB in the serum was detected using quantitative Real Time -PCR. ROC curve analysis was performed to evaluate the diagnostic value of lncRNA-ATB for osteoarthritis. Based on the median serum level of lncRNA-ATB, patients were divided into a high-level group and a low-level group. Correlations between the serum levels of lncRNA-ATB and basic information about the patients were analyzed using the chi-square test. LncRNA-ATB overexpression in human chondrocyte cell line CHON-001 (ATCC CRL2846) was established to study the effects on chondrocyte proliferation (using the CCK-8 assay) and viability. Results: LncRNA-ATB expression was significantly downregulated in the serum of osteoarthritis patients compared with the healthy controls, meaning this downregulation effectively distinguished osteoarthritis patients from healthy subjects. LncRNA-ATB expression in the serum was not significantly affected by the patients’ gender, age or habits, including smoking and alcohol consumption. LncRNA-ATB overexpression activated Akt signaling, promoted proliferation and increased the viability of the chondrocytes. Conclusion: We conclude that downregulation of lncRNA-ATB in serum is a reliable diagnostic marker for osteoarthritis and that this lncRNA participates in the pathogenesis of osteoarthritis by regulating the proliferation and viability of chondrocytes through the activation of Akt signaling.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

23

Opis fizyczny

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Twórcy

autor
  • Xiliang Dang and Liping Lian contributed equally to this work. Second Department of Orthopaedics, Wei Nan Central Hospital, Weinan 714000, Shanxi Province, People’s Republic of China
autor
  • Xiliang Dang and Liping Lian contributed equally to this work. Second Department of Orthopaedics, Wei Nan Central Hospital, Weinan 714000, Shanxi Province, People’s Republic of China
autor
  • Xiliang Dang and Liping Lian contributed equally to this work. Second Department of Orthopaedics, Wei Nan Central Hospital, Weinan 714000, Shanxi Province, People’s Republic of China

Bibliografia

  • 1. Turkiewicz A, Timpka S, Thorlund JB, Ageberg E, Englund M. Knee extensor strength and body weight in adolescent men and the risk of knee osteoarthritis by middle age. Ann Rheum Dis. 2017;76:1657–61.
  • 2. Hare KB, Stefan Lohmander L, Kise NJ, Risberg MA, Roos EM. Middle-aged patients with an MRI-verified medial meniscal tear report symptoms commonly associated with knee osteoarthritis: a cross-sectional study of 199 patients. Acta Orthop. 2017;88:664–9.
  • 3. Kang XZ, Fransen M, Zhang YQ, Li H, Ke Y, Lu M, Su S, Song XY, Guo Y, Chen J, Niu JB, Felson D, Lin JH. The high prevalence of knee osteoarthritis in a rural Chinese population: the Wuchuan osteoarthritis study. Arthritis Rheum. 2009;61:641–7.
  • 4. Zhang Y, Xu L, Nevitt MC, Aliabadi P, Yu W, Qin M, Lui LY, Felson DT. Comparison of the prevalence of knee osteoarthritis between the elderly Chinese population in Beijing and whites in the United States: the Beijing osteoarthritis study. Arthritis Rheum. 2001;44:2065–71.
  • 5. Reid IR. Short-term and long-term effects of osteoporosis therapies. Nat Rev Endocrinol. 2015;11:418–28.
  • 6. Wapinski O, Chang HY. Long noncoding RNAs and human disease. Trends Cell Biol. 2011;21:354–61.
  • 7. Hao L, Fu J, Tian Y, Wu J. Systematic analysis of lncRNAs, miRNAs and mRNAs for the identification of biomarkers for osteoporosis in the mandible of ovariectomized mice. Int J Mol Med. 2017;40:689–702.
  • 8. Zhang C, Wang P, Jiang P, Lv Y, Dong C, Dai X, Tan L, Wang Z. Upregulation of lncRNA HOTAIR contributes to IL-1β-induced MMP overexpression and chondrocytes apoptosis in temporomandibular joint osteoarthritis. Gene. 2016;586:248–53.
  • 9. Su W, Xie W, Shang Q, Su B. The long noncoding RNA MEG3 is downregulated and inversely associated with VEGF levels in osteoarthritis. Biomed Res Int. 2015;2015:35689.
  • 10. Li J, Li Z, Zheng W, Li X, Wang Z, Cui Y, Jiang X. LncRNA-ATB: an indispensable cancer-related long noncoding RNA. Cell Prolif. 2017;47:95–102
  • 11. Sun W, Li Y, Wei S. miR-4262 regulates chondrocyte viability, apoptosis, autophagy by targeting SIRT1 and activating PI3K/AKT/mTOR signaling pathway in rats with osteoarthritis. Exp Ther Med. 2018;15:1119–28.
  • 12. Qu S, Yang X, Song W, Sun W, Li X, Wang J, Zhong Y, Shang R, Ruan B, Zhang Z, Zhang X, Li H. Downregulation of lncRNAATB correlates with clinical progression and unfavorable prognosis in pancreatic cancer. Tumor Biol. 2016;37:3933–8.
  • 13. Shi SJ, Wang LJ, Yu B, Li YH, Jin Y, Bai XZ. LncRNA-ATB promotes trastuzumab resistance and invasion-metastasis cascade in breast cancer. Oncotarget. 2015;6:11652–63.
  • 14. Zhai G, Wang-Sattler R, Hart DJ, Arden NK, Hakim AJ, Illig T, Spector TD. Serum branched-chain amino acid to histidine ratio: a novel metabolomic biomarker of knee osteoarthritis. Ann Rheum Dis. 2010;69:1227–31.
  • 15. Mayfield RD. Emerging roles for ncRNAs in alcohol use disorders. Alcohol. 2017;60:31–9.
  • 16. Wang J, Qiu M, Xu Y, Li M, Dong G, Mao Q, Yin R, Xu L. Long noncoding RNA CCAT2 correlates with smoking in esophageal squamous cell carcinoma. Tumor Biol. 2015;36:5523–8.
  • 17. Enge M, Arda HE, Mignardi M, Beausang J, Bottino R, Kim SK, Quake SR. Single-cell analysis of human pancreas reveals transcriptional signatures of aging and somatic mutation patterns. Cell. 2017;171:321–30 e14.
  • 18. Irizar H, Muñoz-Culla M, Sepúlveda L, Sáenz-Cuesta M, Prada Á, Castillo-Triviño T, Zamora-López G, López de Munain A, Olascoaga J, Otaegui D. Transcriptomic profile reveals gender-specific molecular mechanisms driving multiple sclerosis progression. PLoS One. 2014;9:e90482.
  • 19. Griffin-Walker TG, McKenna KJ, Blair MC, Samy D, White R, Saunders FR, Aspden RM. The roles of NHERF-1 and AKT in osteoarthritis. Osteoarthr Cartil. 2017;25:S153.
  • 20. Xue JF, Shi ZM, Zou J, Li XL. Inhibition of PI3K/AKT/mTOR signaling pathway promotes autophagy of articular chondrocytes and attenuates inflammatory response in rats with osteoarthritis[J]. Biomed Pharmacother. 2017;89:1252–61.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-0fe21991-21a3-4e3b-a81f-762a8738ea58
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