Literature DB >> 31677248

Mesenchymal stem cells in chemotherapy-induced peripheral neuropathy: A new challenging approach that requires further investigations.

Khaled F Al-Massri1, Lamiaa A Ahmed2, Hanan S El-Abhar2.   

Abstract

Chemotherapeutic drugs may disrupt the nervous system and cause chemotherapy-induced peripheral neuropathy (CIPN) as side effects. There are no completely successful medications for the prevention or treatment of CIPN. Many drugs such as tricyclic antidepressants and anticonvulsants have been used for symptomatic treatment of CIPN. Unfortunately, these drugs often give only partial relief or have dose-limiting side effects. Thus, the treatment of CIPN becomes a challenge because of failure to regenerate and repair the injured neurons. Mesenchymal stem cell (MSC) therapy is a new attractive approach for CIPN. Evidence has demonstrated that MSCs play important roles in reducing oxidative stress, neuroinflammation, and apoptosis, as well as mediating axon regeneration after nerve damage in several experimental studies and some clinical trials. We will briefly review the pathogenesis of CIPN, traditional therapies used and their drawbacks as well as therapeutic effects of MSCs, their related mechanisms, future challenges for their clinical application, and the additional benefit of their combination with pharmacological agents. MSCs-based therapies may provide a new therapeutic strategy for patients suffering from CIPN where further investigations are required for studying their exact mechanisms. Combined therapy with pharmacological agents can provide another promising option for enhancing MSC therapy success while limiting its adverse effects.
© 2019 John Wiley & Sons, Ltd.

Entities:  

Keywords:  chemotherapy; neuropathy; regeneration; sciatic nerve; stem cell

Mesh:

Substances:

Year:  2019        PMID: 31677248     DOI: 10.1002/term.2972

Source DB:  PubMed          Journal:  J Tissue Eng Regen Med        ISSN: 1932-6254            Impact factor:   3.963


  6 in total

1.  Reestablishment of Redox Homeostasis in the Nociceptive Primary Afferent as a Mechanism of Antinociception Promoted by Mesenchymal Stem/Stromal Cells in Oxaliplatin-Induced Chronic Peripheral Neuropathy.

Authors:  Anna Lethicia L Oliveira; Gisele G L Santos; Renan F Espirito-Santo; Gessica Sabrina A Silva; Afrânio F Evangelista; Daniela N Silva; Milena B P Soares; Cristiane Flora Villarreal
Journal:  Stem Cells Int       Date:  2021-01-06       Impact factor: 5.443

2.  Pericyte‑derived extracellular vesicles‑mimetic nanovesicles improves peripheral nerve regeneration in mouse models of sciatic nerve transection.

Authors:  Guo Nan Yin; Tae Young Shin; Jiyeon Ock; Min-Ji Choi; Anita Limanjaya; Mi-Hye Kwon; Fang-Yuan Liu; Soon-Sun Hong; Ju-Hee Kang; Yong Song Gho; Jun-Kyu Suh; Ji-Kan Ryu
Journal:  Int J Mol Med       Date:  2021-12-22       Impact factor: 4.101

Review 3.  Targeting strategies for oxaliplatin-induced peripheral neuropathy: clinical syndrome, molecular basis, and drug development.

Authors:  Yang Yang; Bing Zhao; Xuejiao Gao; Jinbing Sun; Juan Ye; Jun Li; Peng Cao
Journal:  J Exp Clin Cancer Res       Date:  2021-10-22

4.  IFN-γ-Primed hUCMSCs Significantly Reduced Inflammation via the Foxp3/ROR-γt/STAT3 Signaling Pathway in an Animal Model of Multiple Sclerosis.

Authors:  Xiao Ling; Teng Wang; Chao Han; Pin Wang; Xiaoli Liu; Chengyun Zheng; Jianzhong Bi; Xiaoyan Zhou
Journal:  Front Immunol       Date:  2022-03-01       Impact factor: 7.561

Review 5.  The Effect of Schwann Cells/Schwann Cell-Like Cells on Cell Therapy for Peripheral Neuropathy.

Authors:  Qian Wang; Fang-Yu Chen; Zhuo-Min Ling; Wen-Feng Su; Ya-Yu Zhao; Gang Chen; Zhong-Ya Wei
Journal:  Front Cell Neurosci       Date:  2022-03-08       Impact factor: 5.505

Review 6.  Chemotherapy-induced peripheral neuropathy-part 2: focus on the prevention of oxaliplatin-induced neurotoxicity.

Authors:  Kinga Sałat
Journal:  Pharmacol Rep       Date:  2020-04-28       Impact factor: 3.919

  6 in total

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