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浆细胞骨髓瘤中的TP53基因多态性

TP53 polymorphism in plasma cell myeloma.

作者信息

Zmorzynski Szymon Andrzej, Korszen-Pilecka Iwona, Wojcierowska-Litwin Magdalena, Kwiatkowska-Drabik Barbara, Luterek Malgorzata, Chocholska Sylwia, Koczkodaj Dorota, Popek Sylwia, Michalak-Wojnowska Malgorzata, Swiderska-Kolacz Grazyna, Januszewska Joanna, Surowiec Iwona, Tomczak Waldemar, Hus Marek, Dmoszynska Anna, Pasiarski Marcin, Poniewierska-Jasak Katarzyna, Cieplinska Katarzyna, Jankowska-Lecka Olga, Filip Agata Anna

机构信息

Department of Cancer Genetics with Cytogenetic Laboratory, Medical University of Lublin, Poland.

出版信息

Folia Histochem Cytobiol. 2017;55(4):203-211. doi: 10.5603/FHC.a2017.0022. Epub 2018 Jan 15.

Abstract

INTRODUCTION

Significant and accessible predictive factors for bortezomib treatment in plasma cell myeloma (PCM) are still lacking. TP53 codon 72 polymorphism (P72R) results in proline (P) or arginine (R) at 72 amino acid position, which causes synthesis of proteins with distinct functions. The aims of our study were to: 1) analyze whether this polymorphism is associated with an increased risk of PCM; 2) study whether the P72R polymorphism affects overall survival (OS) among PCM patients; 3) assess the possible association of the P72R polymorphism with sensitivity to bortezomib in cell cultures derived from PCM patients.

MATERIAL AND METHODS

Genomic DNA from newly diagnosed 59 patients (without IgVH gene rearrangements and TP53 deletions) and 50 healthy blood donors were analyzed by RFLP-PCR to identify TP53 polymorphism. Chromosomal aberrations were detected by use of cIg-FISH. The lymphocyte cell cultures from a subgroup of 40 PCM patients were treated with bortezomib (1, 2 and 4 nM).

RESULTS

The P allele of the P72R polymorphism was more common than the R allele in PMC patients compared to controls (39% vs. 24%), and the difference was significant (p = 0.02). The PP and PR genotypes (in combina-tion) were more frequent among cases than in controls (65% vs. 42%, OR = 2.32, p = 0.04). At the cell culture level and 2 nM bortezomib concentration the PP genotype was associated with higher necrosis rates (10.5%) compared to the PR genotype (5.7%, p = 0.006) or the RR genotype (6.3%, p = 0.02); however, no effect of genotypes was observed at bortezomib concentrations of 1 and 4 nM. The shortest OS (12 months) was observed in patients with the PP genotype compared to patients with the PR or RR genotypes (20 months) (p = 0.04).

CONCLUSIONS

The results suggest that P72R polymorphisms may be associated with an increased PCM risk and may affect OS of PCM patients. However, we saw no consistent results of the polymorphism effect on apoptosis and necrosis in cell cultures derived from PCM patients. Further studies are need in this regard.

摘要

引言

浆细胞骨髓瘤(PCM)中硼替佐米治疗的显著且可获取的预测因素仍然缺乏。TP53基因第72位密码子多态性(P72R)导致72位氨基酸位置上出现脯氨酸(P)或精氨酸(R),这会导致合成具有不同功能的蛋白质。我们研究的目的是:1)分析这种多态性是否与PCM风险增加相关;2)研究P72R多态性是否影响PCM患者的总生存期(OS);3)评估P72R多态性与源自PCM患者的细胞培养物中对硼替佐米的敏感性之间的可能关联。

材料与方法

通过限制性片段长度多态性聚合酶链反应(RFLP-PCR)分析59例新诊断患者(无IgVH基因重排和TP53缺失)及50名健康献血者的基因组DNA,以鉴定TP53多态性。使用cIg-FISH检测染色体畸变。对40例PCM患者亚组的淋巴细胞进行硼替佐米(1、2和4 nM)处理。

结果

与对照组相比,P72R多态性的P等位基因在PCM患者中比R等位基因更常见(39%对24%),差异具有统计学意义(p = 0.02)。病例组中PP和PR基因型(合并)比对照组更常见(65%对42%,OR = 2.32,p = 0.04)。在细胞培养水平和2 nM硼替佐米浓度下,与PR基因型(5.7%,p = 0.006)或RR基因型(6.3%,p = 0.02)相比,PP基因型与更高的坏死率(10.5%)相关;然而,在1 nM和4 nM硼替佐米浓度下未观察到基因型的影响。与PR或RR基因型患者(20个月)相比,PP基因型患者的OS最短(12个月)(p = 0.04)。

结论

结果表明P72R多态性可能与PCM风险增加相关,并可能影响PCM患者的OS。然而,我们在源自PCM患者的细胞培养物中未观察到多态性对凋亡和坏死的一致影响结果。对此需要进一步研究。

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