Journals / Open Journal of Nano / 2023 / Cilt: 8 Sayı: 1

Molecular Docking Study of Midostaurin, an Effective Drug in the Treatment of Myeloid Leukemia

Miyeloid Lösemi Tedavisinde Etkili Bir İlaç Olan Midostaurinin Moleküler Kenetlenme Çalışması

Pages
2–10
Publication Date
2023-06-30
DOI
—
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AI Summary & Key Takeaways

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

The results revealed the significant anti-tumor effect of Midostaurin.

📌 3 Key Takeaways

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Objective & Hypothesis:Midostaurin (C35H30N4O4) is a multi-target kinase inhibitor used to treat some types of acute myeloid leukemia in combination with other chemotherapy agents.
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Key Findings & Data:The conformational analysis of the Midostaurin molecule was performed using the PM3, a semi-experimental method.
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Conclusion & Impact:The results revealed the significant anti-tumor effect of Midostaurin.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Konformasyon analizi · DNA · EGFR

Abstract

Midostaurin (C35H30N4O4) is a multi-target kinase inhibitor used to treat some types of acute myeloid leukemia in combination with other chemotherapy agents. Firstly, the structural preferences of the Midostaurin were evaluated due to the importance to determine the most stable conformer of a bioactive molecule to elucidate its bioactivity. The conformational analysis of the Midostaurin molecule was performed using the PM3, a semi-experimental method. The three most stable conformers and their relative energies were determined. The Epidermal Growth Factor receptor (EGFR) is an integral membrane protein, and its over-expression is associated with the development of a wide variety of tumors. For this reason, EGFR inhibitors can act as anticancer drugs as preventing the growth of EGFR-expressing tumors and increasing the survival rates of patients. On the other hand, DNA is an important target for anticancer drugs. To elucidate the anticancer properties of Midostaurin, the molecular docking simulations were performed against EGFR and DNA targets. The binding modes and binding affinities of the ligand-target receptor complexes were determined. Midostaurin showed strong binding affinity to DNA (G = -8.6 kcal/mol) and EGFR (G = - 9.6 kcal/mol). The results revealed the significant anti-tumor effect of Midostaurin.

Özet

Midostaurin (C35H30N4O4), diğer kemoterapi ajanları ile birlikte bazı akut miyeloid lösemi tiplerini tedavi etmek için kullanılan multi-target kinaz inhibitörüdür. Biyoaktif bir molekülün biyoaktivitesini gösterdiği en kararlı konformerinin belirlenmesinin önemi dolayısıyla ilk olarak Midostaurin’in yapısal tercihleri bulunup değerlendirilmiştir. Midostaurin molekülünün konformasyonel analizi, yarı deneysel bir metot olan PM3 kullanılarak yapılmıştır. En kararlı üç konformer ve bunların bağıl enerjileri belirlenmiştir. Bütünleyici bir zar proteini olan Epitermal Büyüme faktörü reseptörü (EGFR) ve aşırı ekspresyonu, çok çeşitli tümörlerin gelişimi ile ilişkilidir. Bu nedenle, EGFR inhibitörleri, EGFR eksprese eden tümörlerin büyümesini önleyerek ve hastaların hayatta kalma oranlarını artırarak antikanser ilaçlar olarak işlev görebilir. Ek olarak, DNA antikanser ilaçlar için önemli bir hedeftir. Midostaurin’in antikanser özelliklerini aydınlatmak için EGFR ve DNA’ya karşı moleküler kenetlenme simülasyonları yapılmıştır. Ligand-hedef reseptör komplekslerinin bağlanma modları ve bağlanma afiniteleri belirlenmiştir. Midostaurin, DNA (ΔG = -8.6 kcal/mol) ve EGFR (ΔG = - 9.6 kcal/mol) ile güçlü bağlanma afinitesi göstermiştir. Sonuçlar, Midostaurin'in önemli anti-tümör etkisini ortaya çıkarmıştır.

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Cite This Article

ÇELİK, S., YILMAZ, G., ÖZEL, A., AKYÜZ, S. (2023). Molecular Docking Study of Midostaurin, an Effective Drug in the Treatment of Myeloid Leukemia. Open Journal of Nano, Cilt: 8 Sayı: 1, 2–10. https://ajindex.com/articles/911705

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References (12)

  1. Prada-Arismendy, J., Arroyave, J. C., Röthlisberger, S. 2017. Molecular biomarkers in acute myeloid leukemia, Blood reviews 31(1), 63-76
  2. Kumar, C. C. 2011. Genetic abnormalities and challenges in the treatment of acute myeloid leukemia, Genes & cancer 2(2), 95-107
  3. Rubnitz, J. E., Gibson, B., & Smith, F. O. 2008. Acute myeloid leukemia, Pediatric clinics of North America 55(1), 21-51
  4. Schiller, G. J. 2014. Evolving treatment strategies in patients with high-risk acute myeloid leukemia, Leukemia & lymphoma 55(11), 2438-2448
  5. Absalon, M. J., Smith, F. O. 2009. Treatment strategies for pediatric acute myeloid leukemia, Expert opinion on pharmacotherapy 10(1), 57-79
  6. Stone, R. M., Mandrekar, S. J., Sanford, B. L., Laumann, K., Geyer, S., Bloomfield, C. D., Thiede, C., Prior, T.W., Döhner, K., Marcucci, G., Lo-Coco, F., Klisovic, R.B., Wei, A., Sierra, J., Sanz, M.A., Brandwein, J.M., de Witte, T., Niederwieser, D., Appelbaum, F.R., Medeiros, B.C., Tallman, M.S., Krauter, J., Schlenk, R.F., Ganser, A., Serve, H., Ehninger, G., Amadori, S., Larson, R.A., Döhner, H. 2017. Midostaurin plus chemotherapy for acute myeloid leukemia with a FLT3 mutation, New England Journal of Medicine 377(5), 454-464
  7. Schlenk, R. F., Weber, D., Fiedler, W., Salih, H. R., Wulf, G.,. Döhner, H. 2019. Midostaurin added to chemotherapy and continued single-agent maintenance therapy in acute myeloid leukemia with FLT3-ITD, Blood 133(8), 840-851
  8. Levis, M. 2017. Midostaurin approved for FLT3-mutated AML, Blood 129(26), 3403-3406
  9. Stemler, J., Koehler, P., Maurer, C., Müller, C., Cornely, O. A. 2020. Antifungal prophylaxis and novel drugs in acute myeloid leukemia: the midostaurin and posaconazole dilemma, Annals of Hematology 99(7), 1429-1440
  10. Gallogly, M. M., Lazarus, H. M. 2016. Midostaurin: an emerging treatment for acute myeloid leukemia patients, Journal of Blood Medicine 7, 73
  11. Berger, T., Rozovski, U., Moshe, Y., Yaari, S., Frisch, A., Hellmann, I., Apel, A., Aviram, A., Koren-Michowitz, M., Yeshurun, M., Ram, R., Raanani, P., Ofran, Y., Wolach, O. 2019. Midostaurin in combination with intensive chemotherapy is safe and associated with improved remission rates and higher transplantation rates in first remission-a multi-center historical control study, Annals of hematology 98(12), 2711-2717
  12. Patil, Y., Amitay, Y., Ohana, P., Shmeeda, H., Gabizon, A. 2016. Targeting of pegylated liposomal mitomycin-C prodrug to the folate recepto