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Novel α,β-unsaturated hydroxamic acid derivatives overcome cisplatin resistance.
Author: BoesenBenedikt, HamacherAlexandra, Horstick-MucheNadine, KassackMatthias U, KurzThomas, PfliegerMarc, SchrenkChristian, ÖzTaner
Original Abstract of the Article :
A series of α,β-unsaturated hydroxamic acid derivatives as novel HDAC inhibitors (HDACi) with structural modifications of the connecting unit and the CAP group was synthesized. The in vitro evaluation against the human cancer cell lines A2780 and Cal27 identified 6e and 7j as the most pote...See full text at original site
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ラクダ博士は、Health Journal が論文の内容を分かりやすく解説するために作成した架空のキャラクターです。
難解な医学論文を、専門知識のない方にも理解しやすいように、噛み砕いて説明することを目指しています。
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* ラクダ博士は架空のキャラクターであり、実際の医学研究者や医療従事者とは一切関係がありません。
* 解説の内容は Health Journal が独自に解釈・作成したものであり、原論文の著者または出版社の見解を反映するものではありません。
引用元:
https://doi.org/10.1016/j.bmc.2019.07.052
データ提供:米国国立医学図書館(NLM)
Overcoming Cisplatin Resistance: A New Weapon in the Fight Against Cancer
The fight against cancer is an ongoing struggle, like navigating a vast and unforgiving desert. One common challenge is cisplatin resistance, where cancer cells become immune to the effects of this powerful drug. This study presents a promising new approach to overcoming this hurdle, by exploring the potential of α,β-unsaturated hydroxamic acid derivatives as novel HDAC inhibitors (HDACi). These molecules act like a well-timed oasis, offering a new pathway to attack cancer cells.
Synergistic Action Against Cisplatin Resistance
The study found that these new HDACi compounds, specifically 6e and 7j, demonstrated potent HDAC inhibitory activity and effectively inhibited cancer cell proliferation. They were also found to synergistically enhance cisplatin's cytotoxicity, leading to increased apoptosis and caspase-3/7 activation. This synergistic action, like a coordinated desert caravan, effectively targets cancer cells and weakens their resistance to cisplatin.
Potential for Improved Cancer Treatment
These findings offer a glimmer of hope in the fight against cisplatin resistance. The novel dual class I/HDAC6 inhibitors have the potential to improve cancer treatment by overcoming resistance and minimizing side effects compared to existing panobinostat. It's like discovering a new route through the desert, leading to a more effective and less harsh journey toward recovery.
Dr. Camel's Conclusion
This research is a testament to the relentless pursuit of new weapons in the fight against cancer. The discovery of these novel HDACi compounds that effectively overcome cisplatin resistance offers a beacon of hope in the often-harsh landscape of cancer treatment. This breakthrough is a sign that even in the most challenging of deserts, we can find oases of progress and hope.
Date :
- Date Completed 2020-10-20
- Date Revised 2020-10-20
Further Info :
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English
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