Dergiler / Cyprus Journal of Medical Sciences / 2019 / Cilt: 4 - Sayı: 2

The Relationship Between Long Non-Coding RNA Expressions and Ponatinib in Breast Cancer

Sayfa
125–130
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

CONCLUSION The changes in the lncRNA expression profiles and the anti-cancer agent of ponatinib play roles in the definition of therapeutic target for new approach in breast cancer.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:BACKGROUND/AIMS Breast cancer is the most common type of cancer in women and is among the leading causes of cancer-related deaths.
📊
Temel Bulgular & Veri:Long non-coding RNAs (lncRNAs) play significant roles in cell proliferation, transcriptional regulation, cell cycle progression, apoptosis, carcinogenesis, and metastasis.
💡
Sonuç & Katkı:CONCLUSION The changes in the lncRNA expression profiles and the anti-cancer agent of ponatinib play roles in the definition of therapeutic target for new approach in breast cancer.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

BACKGROUND/AIMS Breast cancer is the most common type of cancer in women and is among the leading causes of cancer-related deaths. Long non-coding RNAs (lncRNAs) play significant roles in cell proliferation, transcriptional regulation, cell cycle progression, apoptosis, carcinogenesis, and metastasis. Studies have shown that ponatinib has an antiproliferative effect in some types of cancer. The aim of the present study was to evaluate the effect of ponatinib on cytotoxicity and to determine changes in lncRNA expression levels with the use of ponatinib treatment in estrogen receptor (ER)-independent MDA-MB-231 and ER-dependent MCF-7 breast cancer cells. MATERIAL and METHODS The cytotoxic effects of ponatinib were determined by using the xCELLigence system. Changes in lncRNA expression profiles were determined using quantitative reverse transcription polymerase chain reaction to investigate the antiproliferative roles of ponatinib in breast cancer. RESULTS In human breast adenocarcinoma cell lines (MCF-7 and MDA-MB-231), the IC50 doses of ponatinib were determined to be 4.59 μM (72 h) and 1.41 μM (48 h), respectively. After ponatinib treatment, we observed changes in lncRNA expression profiles in ER-independent MDA-MB-231 and ER-dependent MCF-7 breast cancer cells compared with the control group. CONCLUSION The changes in the lncRNA expression profiles and the anti-cancer agent of ponatinib play roles in the definition of therapeutic target for new approach in breast cancer.

🔖

Bu Makaleye Atıf Yap

OKCANOĞLU, T. B., KAYABAŞI, Ç., SÜSLÜER, S., GÜNDÜZ, C. (2019). The Relationship Between Long Non-Coding RNA Expressions and Ponatinib in Breast Cancer. Cyprus Journal of Medical Sciences, Cilt: 4 - Sayı: 2, 125–130. https://ajindex.com/articles/156884

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (11)

  1. Kilic N, Aras S, Cansaran-Duman D. Determination of Vulpinic Acid Effect on Apoptosis and mRNA Expression Levels in Breast Cancer Cell Lines. Anticancer Agents Med Chem 2018
  2. [CrossRef] 2. Kiliç N, Islakoglu YO, Buyuk İ, Gur-Dedeoglu B, Cansaran-Duman D. Determination of Usnic Acid Responsive miRNAs in Breast Cancer Cell Lines. Anticancer Agents Med Chem 2018. doi: 10.2174/1871520618666181112120142 [Epub ahead of print]. [CrossRef] 3. Miller GD, Bruno BJ, Lim CS. Resistant mutations in CML and Ph(+)ALL - role of ponatinib. Biologics 2014
  3. [CrossRef] 4. Gozgit JM, Wong MJ, Moran L, Wardwell S, Mohemmad QK, Narasimhan NI, et al. Ponatinib (AP24534), a multitargeted panFGFR inhibitor with activity in multiple FGFR-amplified or mutated cancer models. Mol Cancer Ther 2012
  4. [CrossRef] 5. Bauer K, Berger D, Zielinski CC, Valent P, Grunt TW. Hitting two oncogenic machineries in cancer cells: cooperative effects of the multi-kinase inhibitor ponatinib and the BET bromodomain blockers JQ1 or dBET1 on human carcinoma cells. Oncotarget 2018
  5. 26491-506. [CrossRef] 6. Guttman M, Amit I, Garber M, French C, Lin MF, Feldser D, et al. Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals. Nature 2009
  6. [CrossRef] 7. Kung JT, Colognori D, Lee JT. Long noncoding RNAs: past, present, and future. Genetics 2013
  7. [CrossRef] 8. Li J, Liu R, Tang S, Feng F, Wang X, Qi L et al. The effect of long noncoding RNAs HOX transcriptantisense intergenic RNA single‐nucleotidepolymorphisms on breast cancer, cervical cancer, andovarian cancer susceptibility: A meta‐analysis. J Cell Biochem 2018. doi: 10.1002/jcb.27975. [Epub ahead of print]. [CrossRef] 9. Su JC, Hu XF. Long non‑coding RNA HOXA11‑AS promotes cell proliferation and metastasis in human breast cancer. Mol Med Rep 2017
  8. [CrossRef] 10. Russo F, Fiscon G, Conte F, Rizzo M, Paci P, Pellegrini M. Interplay Between Long Noncoding RNAs and MicroRNAs in Cancer. Methods Mol Biol 2018
  9. [CrossRef] 11. Liu H, Li J, Koirala P, Ding X, Chen B, Wang Y, et al. Long non-coding RNAs as prognostic markers in human breast cancer. Oncotarget 2016
  10. 20584-96. [CrossRef] 12. Soudyab M, Iranpour M, Ghafouri-Fard S. The Role of Long Non-Coding RNAs in Breast Cancer. Arch Iran Med 2016
  11. Sun H, Wang G, Peng Y, Zeng Y, Zhu QN, Li TL, et al. H19 lncRNA mediates 17β-estradiol-induced cell proliferation in MCF-7 b