Paper Details 
Original Abstract of the Article :
The Bruton's tyrosine kinase (Btk) inhibitor ibrutinib has demonstrated promising efficacy in a variety of hematologic malignancies. However, the precise mechanism of action of the drug remains to be fully elucidated. Tumor-infiltrating macrophages presented in the tumor microenvironment have been s...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503608/

データ提供:米国国立医学図書館(NLM)

Ibrutinib: A New Weapon in the Desert of Lymphoma

The desert of lymphoma is a formidable landscape, where malignant B cells proliferate, threatening the health of the body. This study examines the promising role of ibrutinib, a Bruton's tyrosine kinase (Btk) inhibitor, in combating this type of cancer.

A New Oasis in the Desert: Ibrutinib's Potential

The study explores the multifaceted mechanisms by which ibrutinib exerts its therapeutic effects. Beyond directly targeting B cells, ibrutinib demonstrates immunomodulatory effects, influencing the behavior of tumor-infiltrating macrophages. By suppressing the production of pro-inflammatory cytokines and chemokines, ibrutinib can effectively disrupt the tumor microenvironment, hindering the growth and spread of lymphoma cells.

Fighting for Survival in the Desert: The Importance of Immunomodulatory Therapies

This study highlights the potential of immunomodulatory therapies, like ibrutinib, to fight cancer by targeting both the malignant cells and the surrounding environment. This approach offers a promising avenue for treating lymphoma and potentially other cancers, providing new hope for patients battling these devastating diseases.

Dr.Camel's Conclusion

This study is like finding a new weapon in the desert of lymphoma. Ibrutinib's immunomodulatory effects, in addition to its direct cytotoxic action, offer a promising approach to fighting this type of cancer. It is a beacon of hope in the ongoing search for effective cancer treatments.

Date :
  1. Date Completed 2018-06-07
  2. Date Revised 2021-12-04
Further Info :

Pubmed ID

28424405

DOI: Digital Object Identifier

PMC5503608

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Languages

English

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