Journals / Turkish Journal of Medical Sciences / 2017 / Cilt: 47 - Sayı: 1

Identification of the cysteine-rich 61 (CYR61) gene variations in osteosarcoma patients

Pages
284–294
Publication Date
2022-11-05
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The overall CYR61 variation frequency in exons 2, 3, 4, and 5 was determined to be 46.55% (27/58).

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Background/aim: Osteosarcoma requires an angiogenesis process.
📊
Key Findings & Data:CYR61 is one of the extracellular signaling molecules that promote angiogenesis, tumor growth, and the malignancy of osteosarcoma.
💡
Conclusion & Impact:The overall CYR61 variation frequency in exons 2, 3, 4, and 5 was determined to be 46.55% (27/58).
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Background/aim: Osteosarcoma requires an angiogenesis process. CYR61 is one of the extracellular signaling molecules that promote angiogenesis, tumor growth, and the malignancy of osteosarcoma. In the present study, we investigate the CYR61 gene variations in osteosarcoma and their correlations with clinicopathological findings. Materials and methods: We performed variation analysis of the CYR61 gene in 58 patients with osteosarcoma. With an aim to ascertain the variety of variations in exons 2, 3, 4, and 5 of the CYR61 gene in osteosarcoma, we did a PCR-SSCP followed by DNA sequencing. Results: In osteosarcoma the CYR61 gene variations found were 18.96% (11/58) in exon 2, 3.44% (2/58) in exon 3, 8.62% (5/58) in exon 4, and 15.51% (9/58) in exon 5. In our variation analysis, we detected one missense variation in exon 2 (Arg47Trp), one silent variation in exon 3 (Lys152Lys), one missense variation in exon 4 (Phe213Leu), and two missense variations in exon 5 (Gly315Arg and Asp339Asn). The overall CYR61 variation frequency in exons 2, 3, 4, and 5 was determined to be 46.55% (27/58). Conclusion: Our study specifies the role of CYR61 gene variation in osteosarcoma. The result signifies that CYR61 might be used as a prognostic/diagnostic marker in osteosarcoma patients.

🔖

Cite This Article

KUMAR, V., SINGH, A., KUMAR, V., HUSSAIN, S. R., MAHDI, A. A., ALI, S., RIZIVI, N., YADAV, M., AHMAD, M. K. (2022). Identification of the cysteine-rich 61 (CYR61) gene variations in osteosarcoma patients. Turkish Journal of Medical Sciences, Cilt: 47 - Sayı: 1, 284–294. https://ajindex.com/articles/610964

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (14)

  1. Harada S, Rodan GA. Control of osteoblast function and regulation of bone mass. Nature 2003; 15: 349-355
  2. Stiller CA. International patterns of cancer incidence in adolescents. Cancer Treat Rev 2007; 33: 631-645
  3. Coventry MB, Dahlin DC. Osteogenic sarcoma - A critical analysis of 430 cases. J Bone Joint Surg Am 1957; 39: 741-757
  4. Marcove RC, Mike V, Hajek JV, Levin AG, Hutter RV. Osteogenic sarcoma under the age of twenty-one. A review of one hundred and forty-five operative cases. J Bone Joint Surg Am 1970; 52: 411-423
  5. Bielack S, Carrle D, Casali PG; ESMO Guidelines Working Group. Osteosarcoma: ESMO clinical recommendations for diagnosis, treatment and follow-up. Ann Oncol 2009; 20 (Suppl. 4): 137-139
  6. Tang N, Song WX, Luo J, Haydon RC, He TC. Osteosarcoma development and stem cell differentiation. Clin Orthop Relat Res 2008; 466: 2114-2130 7. Damron TA, Ward WG, Stewart A. Osteosarcoma, chondrosarcoma, and Ewing’s sarcoma: National Cancer Data Base Report. Clin Orthop Relat Res 2007; 459: 40-47
  7. Kireeva ML, MO FE, Yang GP, Lau LF. CYR61, a product of a growth factor-inducible immediate-early gene, promotes cell proliferation, migration, and adhesion. Mol Cell Biol 1996; 16: 1326-1334
  8. Ries LAG, Smith MA, Gurney JG, Linet M, Tamra T, Young JL, Bunin GR. Cancer Incidence and Survival among Children and Adolescents: United States SEER Program 1975-1995. Bethesda, MD, USA: National Cancer Institute, SEER Program; 1999
  9. Omololu AB, Ogunbiyi JO, Ogunlade SO, Alonge TO, Adebisi A, Akang EE. Primary malignant bone tumour in a tropical African University teaching hospital. West Afr J Med 2002; 21: 291-293
  10. Chen PC, Cheng HC, Yang SF, Lin CW, Tang CH. The CCN family proteins: modulators of bone development and novel targets in bone-associated tumors. Biomed Res Int 2014; 2014: 437096
  11. Tan TW, Huang YL, Chang JT, Lin JJ, Fong YC, Kuo CC, Tsai CH, Chen YJ, Hsu HC, Cho DY et al. CCN3 increases BMP4 expression and bone mineralization in osteoblasts. J Cell Physiol 2012; 227: 2531-2541
  12. O’Brien TP, Yang GP, Sanders L, Lau LF. Expression of CYR61, a growth factor inducible immediate-early gene. Mol Cell Biol 1990; 10: 3569-3577
  13. Frazier K, Williams S, Kothapalli D, Klapper H, Grotendorst GR. Stimulation of fibroblast cell growth, matrix production, and granulation tissue formation by connective tissue growth factor. J Invest Dermatol 1996; 107: 404-411
  14. Chen N, Chen CC, Lau LF. CYR61, a product of a growth factor-inducibl