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Sci Rep:亚洲前列腺癌患者中周围血栓栓塞性血管疾病与雄激素阻断治疗相关性分析

2019-10-12 AlexYang MedSci原创

最近,有研究人员在前列腺癌(PCa)患者中调查了血栓栓塞的血管疾病在雄激素阻断治疗(ADT)后的风险情况。研究包括了24464名在2000-2008年新诊断为PCa的患者,且是通过纵向医疗保险数据库获得数据。所有的的PCa患者分成了2组:ADT组和非ADT组。ADT治疗的患者再分成手术去势组,化学去势组和单独抗雄激素组。研究人员通过依赖时间变量的多重Cox比例风险回归评估了肺栓塞(PE)、外周动脉

最近,有研究人员在前列腺癌(PCa)患者中调查了血栓栓塞的血管疾病在雄激素阻断治疗(ADT)后的风险情况。

研究包括了24464名在2000-2008年新诊断为PCa的患者,且是通过纵向医疗保险数据库获得数据。所有的的PCa患者分成了2组:ADT组和非ADT组。ADT治疗的患者再分成手术去势组,化学去势组和单独抗雄激素组。研究人员通过依赖时间变量的多重Cox比例风险回归评估了肺栓塞(PE)、外周动脉闭塞症(PAOD)和深静脉血栓形成(DVT)的风险。在12年的跟踪调查期间,ADT组和非ADT组中每1000人DVT的发生率分别为2.87和1.62;PE的发生率分别为1.00和0.52;PAOD的发生率分别为1.03和0.70。另外,与对应的ADT未接受患者相比,DVT和PE的风险在接受组合雄激素阻断(CAB)的患者中显著增加。在调整了潜在的风险因子后,接受CAB治疗的PCa患者具有最高的PE风险(HR=3.11),之后是DVT风险(HR=2.53)。DVT风险在整个化学去势中提高。然而,高PE风险在接受不大于720天治疗的患者中也存在。研究人员并未发现ADT和PAOD风险的相关性。

最后,研究人员指出,PE和DVT的风险在接受CAB治疗的亚洲PCa患者中较高,而PAOD风险与这些治疗没有关系。

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    2019-10-12 misszhang

    前列腺癌相关研究,学习了,谢谢梅斯

    0

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Nat Med:全基因组种系与前列腺癌表观遗传背景相关

肿瘤的发生可以由种系、环境和随机因素诱发。但这些因素是怎样互作产生肿瘤的分子表型的仍旧未知。最近,有研究人员在589个局部前列腺肿瘤中量化了种系多样性对体细胞表观基因组的影响。研究发现,倾向性风险位点影响了肿瘤的表观基因组,揭示了癌症易感性的机制。研究人员总共见顶了1178个位点与肿瘤组织中甲基化的改变有关,而不是非恶性肿瘤组织。这些肿瘤甲基化数量性状位点能够影响染色质结构以及RNA和蛋白的丰度。

Sci Rep:病灶间的异质性挑战了分子分型在原发性前列腺癌中的临床使用

前列腺癌是高度异质性的疾病,并且在起始诊断时往往具有典型的多个不同的癌症病灶。前列腺癌的分子分型能够游离的辅助精准的诊断和治疗。在癌症基因组数据库(TCGA)中公开了一个很有前景的分型工具,并基于每个患者的癌症样本成功的对74%的原发性前列腺癌分型,共分成了7组。最近,有研究人员探索了该分型工具的临床使用情况,他们在一个多病灶的背景下对该分型工具进行了测试。研究人员共分析了来自于39名患者的85个

Nat Commun:PTEN-ARID4B-PI3K途径鉴定了PTEN缺陷前列腺癌对ARID4B的依赖性

在前列腺癌中,PTEN经常发生变异。PTEN的肿瘤抑制子功能归结于其脂肪磷酸化活性且能够拮抗PI3K的作用。最近,有研究人员报道了PTEN-ARID4B-PI3K途径,其中PTEN能够抑制ARID4B的表达,而ARID4B是PI3K亚单元基因PIK3CA和PIK3R2的转录激活因子,且亚单元基因PIK3CA和PIK3R2对PI3K/AKT途径的激活是非常关键的。ARID4B和组蛋白H1结合到PIK

Sci Rep:前列腺癌细胞中AR无差异抗雄激素抗性驱使因子分析

二代抗雄激素类药物抑制雄激素受体(AR)是转移去势抵抗性前列腺癌(mCRPC)的标准治疗方法,但是不可避免的会导致抗性的产生。自从高效AR信号抑制剂的使用,大于20%的mCRPC的患者发展为不依赖AR抗性机制疾病。最近,有研究人员开发了2个抗雄激素药物和不依赖AR活性的去势抵抗性前列腺癌细胞模型,尽管模型中AR表达强烈(AR无差异)。这些模型对所有当今的AR信号抑制剂存在抗性。研究发现,这2个细胞

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