Depletion of nerve growth factor in chemotherapy-induced peripheral neuropathy associated with hematologic malignancies

被引:24
|
作者
Youk, Jeonghwan [1 ]
Kim, Young-Sook [2 ]
Lim, Jung-Ah [2 ]
Shin, Dong-Yeop [1 ]
Koh, Youngil [1 ]
Lee, Soon-Tae [2 ]
Kim, Inho [1 ,3 ]
机构
[1] Seoul Natl Univ Hosp, Dept Internal Med, Div Hematol Oncol, Seoul, South Korea
[2] Seoul Natl Univ Hosp, Dept Neurol, Seoul, South Korea
[3] Seoul Natl Univ, Canc Res Inst, Coll Med, Seoul, South Korea
来源
PLOS ONE | 2017年 / 12卷 / 08期
基金
新加坡国家研究基金会;
关键词
CISPLATIN NEUROTOXICITY; SENSORY NEUROPATHY; TRIAL; PAIN; MICE; TAXOL; RATS; CARBOPLATIN; PREDICTORS; PACLITAXEL;
D O I
10.1371/journal.pone.0183491
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective To investigate whether the depletion of nerve growth factor (NGF) is associated with the development of chemotherapy-induced peripheral neuropathy (CIPN) in patients with hematologic malignancy. Methods We prospectively enrolled hematologic cancer patients who had a plan to receive bortezomib, thalidomide, or vincristine. Baseline NGF levels were measured within one week before the start date of chemotherapy. Follow-up NGF levels were measured after four months from the start date of chemotherapy or the date when CIPN was initially diagnosed. Results Baseline and follow-up NGF pairs were measured in 45 patients (male/female = 27/18, median age = 63 years old). CIPN has developed in 28 patients. In the CIPN group, the level of NGF was significantly decreased after chemotherapy compared to the baseline (Delta NGF = -3.52 +/- 5.72; p-value = 0.003), while the NGF level of the no-CIPN group was not changed after chemotherapy. The differences in Delta NGF levels between the CIPN and no-CIPN group were more profound when analyzed in the subgroup of newly diagnosed multiple myeloma patients (Delta NGF = -4.14 +/- 4.87 pg/ml for the CIPN group and +2.52 +/- 8.39 pg/ml for the no-CIPN group; p-value = 0.043). Conclusions This study shows that the depletion of NGF occurs during the development of CIPN, suggesting pathogenesis based on the role of NGF and therapeutic implications.
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页数:11
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