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首页> 外文期刊>Medicine. >Interleukin-6 gene-174 G/C promoter polymorphism is not associated with multiple myeloma susceptibility: evidence from meta-analysis
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Interleukin-6 gene-174 G/C promoter polymorphism is not associated with multiple myeloma susceptibility: evidence from meta-analysis

机译:白细胞介素-6基因-174g / c启动子多态性与多种骨髓瘤敏感性无关:来自Meta分析的证据

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Multiple myeloma [1,2,3,4] (MM) isa group ofmalignant plasmacellclonal diseases, with thecancercells thereof being derived fromthe plasma cells,and plasmacells [5] being thecells inwhichBlymphocytes [6] growto the ultimatefunctionalstage. The primary feature ofMMisabnormal proliferation of bone marrowplasmacells [7] with excessive production ofmonoclonalimmunoglobulin [8] or lightchain (Mprotein), [9,10] resulting in terminal organ damage. Theevolution ofMMis heterogeneous,and thesurvivaltime of patients with invasive manifestations isestimated to beless than 1 year. [11,12] Previous data highlighted that theincidence ofMMaccounts forabout 1%ofallsystemmalignant tumors, [13,14] often occurring inmiddle-aged and elderly patients, with theclinicalmanifestations thereof being complex and diverse, potentially causing anemia, infection, bleeding, bone pain,and even fracture. Alongwith theaforementioned issues, MMcould even lead to rareclinicalsymptoms, such as signs of nerveroot irritation. [15] As reported by existing research, theincidence ofmultiple myeloma has progressively increased worldwide over the past fewdecades, [16–18] substantially affecting the quality oflife of peopleand increasing the medicaland health burden ofsociety.
机译:多发性骨髓瘤[1,2,3,4](mm)ISA组的靶向疟原虫疾病,其源自血浆细胞衍生自血浆细胞,并且Plasmacells [5]是含有血管素[6]的血管素[6]生长。骨髓骨髓增殖的主要特征[7]用过多的Manoclonimmunogloglobulin [8]或灯链(Mprotein),[9,10],导致末端器官损伤。 MMIS异质的分析,患有侵袭性表现患者的患者令人生畏的患者患有1年。 [11,12]以前的数据突出显示,MMAccounts forabout的抗效性1%常绿症,[13,14]通常发生inmiddle-yaned和老年患者,其inclinalmanifistations是复杂和多样化的,可能导致贫血,感染,出血,骨痛,甚至骨折。沿着卑鄙的问题,甚至会导致RareclinalSymptoms,如Nerveroot刺激的迹象。 [15]正如现有研究所报道的那样,Multiple骨髓瘤的抗效在过去几十个世纪逐渐增加了全世界,[16-18]基本上影响了人类的品质,增加了医疗和社会医疗保健负担。

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