Paper Details 
Original Abstract of the Article :
Pazopanib and lapatinib are two tyrosine kinase inhibitors that have been designed to inhibit the VEGF tyrosine kinase receptors 1, 2 and 3 (pazopanib), and the HER1 and HER2 receptors in a dual manner (lapatinib). Pazopanib has also been reported to mediate inhibitory effect on a selected panel of ...See full text at original site
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引用元:
https://doi.org/10.1038/onc.2009.277

データ提供:米国国立医学図書館(NLM)

Synergistic Proapoptotic Effects of Pazopanib and Lapatinib

[Cancer] is a complex and multifaceted disease, and finding effective treatments remains a crucial goal. This research explores the potential of combining two tyrosine kinase inhibitors, [pazopanib] and [lapatinib], to synergistically induce apoptosis in cancer cells.

Synergistic Anti-Cancer Effects: Combining Tyrosine Kinase Inhibitors

The study demonstrates that [pazopanib] and [lapatinib] act synergistically to [induce apoptosis] in [A549 non-small-cell lung cancer cells]. This synergistic effect was observed across a panel of unrelated human carcinoma cell lines, suggesting the potential of this combination therapy for treating various types of cancer.

Fighting Cancer: The Power of Combination Therapy

This research highlights the potential of [combination therapy] in enhancing cancer treatment efficacy. Just as a camel relies on multiple adaptations to thrive in the desert, we can leverage multiple therapeutic approaches to combat cancer. This study underscores the importance of exploring synergistic combinations of drugs to improve patient outcomes and enhance the fight against cancer.

Dr. Camel's Conclusion

Cancer research constantly seeks new and innovative ways to combat this devastating disease. This study demonstrates the potential of [combination therapy] using [pazopanib] and [lapatinib] to synergistically induce apoptosis in cancer cells, offering a promising new avenue for cancer treatment.
Date :
  1. Date Completed 2010-01-06
  2. Date Revised 2021-12-03
Further Info :

Pubmed ID

19749798

DOI: Digital Object Identifier

10.1038/onc.2009.277

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Languages

English

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