UGC Approved Journal no 63975(19)
New UGC Peer-Reviewed Rules

ISSN: 2349-5162 | ESTD Year : 2014
Volume 13 | Issue 3 | March 2026

JETIREXPLORE- Search Thousands of research papers



WhatsApp Contact
Click Here

Published in:

Volume 11 Issue 12
December-2024
eISSN: 2349-5162

UGC and ISSN approved 7.95 impact factor UGC Approved Journal no 63975

7.95 impact factor calculated by Google scholar

Unique Identifier

Published Paper ID:
JETIR2412129


Registration ID:
551985

Page Number

b334-b345

Share This Article


Jetir RMS

Title

Advancements and Challenges in Multiple Myeloma: Insights into Bone Marrow Pathophysiology and Therapeutic Strategies

Abstract

Apoptosis, survival, proliferation, invasion, and other biological characteristics of the malignant phenotype are all influenced by pathophysiological interactions with microenvironmental components in multiple myeloma, a B-cell lineage cancer in which neoplastic plasma cells proliferate in the bone marrow. Multiple myeloma (MM) is still incurable, even though patient survival has improved over the past 20 years due to the development of a safer and more effective class of medications (such as immunomodulators, proteasome inhibitors, and monoclonal antibodies). Tumour plasma cells settle and proliferate in the complex structure known as the bone marrow microenvironment, which is made up of cells, extracellular matrix (ECM) proteins, and cytokines. Because tumour plasma cell-induced alteration is essential for creating a “permissive” environment that promotes MM plasma cell proliferation, migration, survival, and treatment resistance, the bone marrow (BM) microenvironment plays a critical role in the course of MM illness. The multiple myeloma microenvironment’s “activated phenotype” contributes to plasma cell treatment resistance as well as proliferation and dissemination. Autophagy, transcriptional rewiring, stress-managing pathways, and dysregulation of non-coding RNAs are the mechanisms via which bone marrow stromal cells create drug resistance in plasma cells. These mechanisms serve as new targets for the growing arsenal of anti-MM treatment options.

Key Words

Multiple myeloma; biological models; bone marrow; 3D printing, plasma cells.

Cite This Article

"Advancements and Challenges in Multiple Myeloma: Insights into Bone Marrow Pathophysiology and Therapeutic Strategies", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.11, Issue 12, page no.b334-b345, December-2024, Available :http://www.jetir.org/papers/JETIR2412129.pdf

ISSN


2349-5162 | Impact Factor 7.95 Calculate by Google Scholar

An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 7.95 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator

Cite This Article

"Advancements and Challenges in Multiple Myeloma: Insights into Bone Marrow Pathophysiology and Therapeutic Strategies", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.11, Issue 12, page no. ppb334-b345, December-2024, Available at : http://www.jetir.org/papers/JETIR2412129.pdf

Publication Details

Published Paper ID: JETIR2412129
Registration ID: 551985
Published In: Volume 11 | Issue 12 | Year December-2024
DOI (Digital Object Identifier):
Page No: b334-b345
Country: vaijapur , Maharashtra , India .
Area: Pharmacy
ISSN Number: 2349-5162
Publisher: IJ Publication


Preview This Article


Downlaod

Click here for Article Preview

Download PDF

Downloads

000208

Print This Page

Current Call For Paper

Jetir RMS