Literature DB >> 18774880

Pathophysiological underpinnings of multiple myeloma progression.

Sundar Jagannath1.   

Abstract

BACKGROUND: Multiple myeloma (MM) is a malignant neoplasm of plasma cells that accumulate in the bone marrow. Myeloma is characterized by skeletal destruction, renal failure, hypercalcemia, and anemia. Currently, there is no cure, though recent understanding of the bone marrow microenvironment and the cytogenetics involved in MM are leading to improved and individualized treatment strategies, leading to longer periods of remission and improved survival rates.
OBJECTIVE: To review MM pathophysiology, genetic issues, other risk factors, and the steps of disease progression. This section will address diagnosis, staging, classification, and disease complications, as well as the roles of cytogenetic abnormalities and the bone marrow milieu.
SUMMARY: In MM, malignant plasma cells in the in the bone marrow produce large quantities of monoclonal protein (M protein) leading to stimulation of osteoclasts. This increase in osteoclast activity leads to bone resorption and destruction, causing painful bone lesions and hypercalcemia. Myeloma cells also crowd out other normal bone marrow cells, which leads to a plethora of complications, including renal insufficiency, anemia, infection, and clotting disorders. Updated standards of diagnosis, staging, and classification of MM have recently been developed. The International Staging System (ISS) categorizes myeloma patients into 1 of 3 groups based on serum albumin and beta2-microglobulin blood tests. Genetic mutations leading to chromosomal translocations and deletions play a key role in the progression to active, malignant MM. Cytogenetic testing allows physicians to appropriately diagnose and treat patients specific to their unique presentation of disease.
CONCLUSION: The future of treating the myeloma patient is progressing at a fast and positive pace. Identification and treatment of comorbid conditions are leading to improvements in quality of life. Identification of potential therapeutic targets in the bone marrow microenvironment is leading to the development of therapies that are changing the standard of care for MM patients.

Entities:  

Mesh:

Year:  2008        PMID: 18774880     DOI: 10.18553/jmcp.2008.14.S7-A.7

Source DB:  PubMed          Journal:  J Manag Care Pharm        ISSN: 1083-4087


  4 in total

1.  Heparanase enhances local and systemic osteolysis in multiple myeloma by upregulating the expression and secretion of RANKL.

Authors:  Yang Yang; Yongsheng Ren; Vishnu C Ramani; Li Nan; Larry J Suva; Ralph D Sanderson
Journal:  Cancer Res       Date:  2010-10-26       Impact factor: 12.701

2.  Runx2 Suppression by miR-342 and miR-363 Inhibits Multiple Myeloma Progression.

Authors:  Pramod S Gowda; Benjamin J Wildman; Timothy N Trotter; Xiaoxuan Xu; Xiaoxiao Hao; Mohammad Q Hassan; Yang Yang
Journal:  Mol Cancer Res       Date:  2018-03-28       Impact factor: 5.852

3.  Myeloma cell-derived Runx2 promotes myeloma progression in bone.

Authors:  Timothy N Trotter; Mei Li; Qianying Pan; Deniz Peker; Patrick D Rowan; Juan Li; Fenghuang Zhan; Larry J Suva; Amjad Javed; Yang Yang
Journal:  Blood       Date:  2015-04-10       Impact factor: 22.113

4.  Heparanase inhibits osteoblastogenesis and shifts bone marrow progenitor cell fate in myeloma bone disease.

Authors:  Jian Ruan; Timothy N Trotter; Li Nan; Rongcheng Luo; Amjad Javed; Ralph D Sanderson; Larry J Suva; Yang Yang
Journal:  Bone       Date:  2013-07-27       Impact factor: 4.398

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.