Paper Details 
Original Abstract of the Article :
Head and neck squamous cell carcinoma (HNSCC) is an aggressive and often fatal disease. Cisplatin is the most common chemotherapeutic drug in the treatment of HNSCC, but intrinsic and acquired resistance are frequent, and severe side effects occur at high doses. The second messenger cyclic GMP (cGMP...See full text at original site
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引用元:
https://pubmed.ncbi.nlm.nih.gov/28025101

データ提供:米国国立医学図書館(NLM)

Soluble Guanylate Cyclase Stimulators: Enhancing Cisplatin's Impact in Head and Neck Cancer

This research explores the potential of soluble guanylate cyclase (sGC) stimulators in enhancing the effectiveness of cisplatin, a common chemotherapy drug used to treat head and neck squamous cell carcinoma (HNSCC). HNSCC is an aggressive cancer with a high risk of recurrence, and finding ways to improve treatment outcomes is crucial. The study investigated the synergistic effects of sGC stimulators and cisplatin in reducing HNSCC cell viability and promoting apoptosis.

A New Approach to Cancer Treatment

The study revealed that sGC stimulators, when combined with cisplatin, significantly reduced HNSCC cell viability and enhanced apoptosis. Importantly, the sGC stimulators also demonstrated efficacy in overcoming cisplatin resistance, a major challenge in HNSCC treatment.

A Potential Boost for Cancer Therapy

The findings suggest that sGC stimulators could represent a valuable addition or alternative to cisplatin in the treatment of HNSCC. These drugs have the potential to improve treatment outcomes and potentially reduce the need for higher doses of cisplatin, minimizing the risk of severe side effects.

Dr. Camel's Conclusion

Imagine a camel traveling through a desert, seeking a way to overcome a challenging obstacle. SGC stimulators, when combined with cisplatin, act like a powerful ally, helping to combat HNSCC more effectively. This research offers hope for new strategies to improve the treatment of this aggressive cancer.
Date :
  1. Date Completed 2017-08-08
  2. Date Revised 2019-02-21
Further Info :

Pubmed ID

28025101

DOI: Digital Object Identifier

NIHMS841793

Related Literature

SNS
PICO Info
in preparation
Languages

English

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