Paper Details 
Original Abstract of the Article :
Multiple myeloma (MM) is a hematological malignancy that is characterized by the clonal expansion of plasma cells in the bone marrow. Histone deacetylases (HDACs) represent a new type of molecular targeted therapy for different types of cancers and promising targets for myeloma therapy. We showed th...See full text at original site
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引用元:
https://doi.org/10.1097/CAD.0000000000000568

データ提供:米国国立医学図書館(NLM)

Targeting Histone Deacetylases in Multiple Myeloma: A New Path to Treatment

Multiple myeloma, a cancer of plasma cells, is a formidable adversary, like a relentless sandstorm threatening the body's delicate balance. This study explores a new approach to treating multiple myeloma, targeting histone deacetylases (HDACs) with a novel inhibitor, BG45. The researchers investigated the effects of BG45 on multiple myeloma cells in vitro, hoping to find a way to effectively combat this disease.

HDAC Inhibition: A New Weapon in the Arsenal Against Multiple Myeloma

This research suggests that targeting HDACs with inhibitors like BG45 may offer a promising new avenue for treating multiple myeloma. The findings indicate that BG45 effectively inhibits the growth and induces apoptosis in multiple myeloma cells, showcasing its potential as a therapeutic agent.

Combating Cancer with Precision: A New Frontier in Myeloma Treatment

This study highlights the potential of HDAC inhibitors like BG45 to revolutionize the treatment of multiple myeloma, offering a targeted and potentially more effective approach. The findings encourage further research into this promising area of cancer therapy.

Dr. Camel's Conclusion

Just as a camel uses its keen senses to navigate the desert, BG45 targets specific molecules within cancer cells, disrupting their growth and ultimately leading to their demise. This research offers a glimpse into the potential of HDAC inhibitors to reshape the landscape of multiple myeloma treatment.

Date :
  1. Date Completed 2018-05-10
  2. Date Revised 2018-12-02
Further Info :

Pubmed ID

29049036

DOI: Digital Object Identifier

10.1097/CAD.0000000000000568

Related Literature

SNS
PICO Info
in preparation
Languages

English

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