Mol Neurobiol:新的治疗方法或可有效对抗胶质母细胞瘤

2016-09-27 MedSci MedSci原创

胶质母细胞瘤是原发性恶性脑肿瘤最常见的形式。这些肿瘤具有高度增殖和浸润性,导致患者诊断后的中位生存期仅为14个月。目前的治疗方案对癌干细胞存在于肿瘤性微环境中的一小部分患者来说是无效的;然而,一种新的治疗方法或可在维持肿瘤干细胞表型的情况下将其移除至这种微环境的外面。 在体外研究人员已从人高级别胶质瘤(胶质瘤细胞球形成细胞(GSCs))中分离出多能成球细胞来研究这些细胞的粘附和迁移特性。由于

胶质母细胞瘤是原发性恶性脑肿瘤最常见的形式。这些肿瘤具有高度增殖和浸润性,导致患者诊断后的中位生存期仅为14个月。目前的治疗方案对癌干细胞存在于肿瘤性微环境中的一小部分患者来说是无效的;然而,一种新的治疗方法或可在维持肿瘤干细胞表型的情况下将其移除至这种微环境的外面。

在体外研究人员已从人高级别胶质瘤(胶质瘤细胞球形成细胞(GSCs))中分离出多能成球细胞来研究这些细胞的粘附和迁移特性。由于其在胶质母细胞瘤和GSCs中高度表达及激活细胞因子和生长因子的能力,研究人员重点专注了两个密切相关的基质金属蛋白酶ADAM10和ADAM17的作用。

结果发现,选择性抑制ADAM10和ADAM17 GSC的表达可增加GSC,但是并没有增加神经干细胞的增殖和迁移,且迁移的GSCs具有分化表型。

此外,研究人员还观察到Nestin,干/祖细胞标记物和纤连蛋白(一种在高级别胶质瘤组织中的表达的细胞外基质蛋白)之间存在关联。GSCs对纤维连接蛋白的粘附是由α5β1整合素介导的,纤维连接蛋白进一步促进GSC的迁移,且可促进体内肿瘤干细胞迁移出肿瘤性微环境。

总而言之,该研究结果表明,针对ADAM10和ADAM17的治疗或可促进癌干细胞迁移并远离肿瘤微环境,由此可使得肿瘤细胞分化为更容易治疗的表型.

原始出处:

Elodie J. Siney. Et al., Metalloproteinases ADAM10 and ADAM17 Mediate Migration and Differentiation in Glioblastoma Sphere-Forming Cells. Mol Neurobiol. 19 August 2016. DOI: 10.1007/s12035-016-0053-6.

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    2017-04-25 sunylz
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    2016-10-05 等你一年又一年

    应该学习,继续研究

    0

  6. 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  7. 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  8. 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likeNumber=61, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=https://wx.qlogo.cn/mmopen/mStl88fu4NfdY7yem1P7bRvOP6z0jKsBoYR8ezfAricY7meQWcte7LRJsWHVn0CnPJg2JuQmevR0DoFmmEib5QLD2kNESBESQT/0, createdBy=59191706502, createdName=医路开来, createdTime=Tue Sep 27 14:16:11 CST 2016, time=2016-09-27, status=1, ipAttribution=)]
    2016-09-28 oo902

    这是一种全新的方法

    0

  9. 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likeNumber=61, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=https://wx.qlogo.cn/mmopen/mStl88fu4NfdY7yem1P7bRvOP6z0jKsBoYR8ezfAricY7meQWcte7LRJsWHVn0CnPJg2JuQmevR0DoFmmEib5QLD2kNESBESQT/0, createdBy=59191706502, createdName=医路开来, createdTime=Tue Sep 27 14:16:11 CST 2016, time=2016-09-27, status=1, ipAttribution=)]
    2016-09-28 正准备

    好难,继续继续

    0

  10. 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likeNumber=61, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=https://wx.qlogo.cn/mmopen/mStl88fu4NfdY7yem1P7bRvOP6z0jKsBoYR8ezfAricY7meQWcte7LRJsWHVn0CnPJg2JuQmevR0DoFmmEib5QLD2kNESBESQT/0, createdBy=59191706502, createdName=医路开来, createdTime=Tue Sep 27 14:16:11 CST 2016, time=2016-09-27, status=1, ipAttribution=)]
    2016-09-27 医路开来

    :新的治疗方法或可有效对抗胶质母细胞瘤

    0

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最近有一位来自法国巴黎萨伯特慈善医院的神经外科医生Alexandre Carpentier,以第一作者的身份在《科学》杂志的子刊《转化医学》上发表了文章,他带领的团队开发了一种超声装置,对15名出现复发性胶质母细胞瘤病人进行了实验装置检测,目的在于突破血脑屏障,帮助化疗药物到达脑部。  所以,什么是血脑屏障呢?我们为什么要打开它?实际上,血脑屏障并不是环绕在大脑四周的「护城墙」

Oncotarget:新研究找到让致命脑瘤发生萎缩的重要分子

  (图片来自UC San Diego Health) 患胶质母细胞瘤的病人一般在诊断后存活时间不超过15个月,目前仍然没有治疗这一绝症的有效方法。最近,来自美国加州大学圣地亚哥分校的研究人员开发了一种能够用于筛选胶质母细胞瘤治疗药物的新方法,他们利用这一方法发现了一种能够使肿瘤平均尺寸减小一半的重要分子。相关研究结果发表在国际学术期刊Oncotarget上。  

JAMA:治疗胶质母细胞瘤——TTFields加替莫唑胺效果改善显著

胶质母细胞瘤是成人中枢神经系统的的最具破坏性的原发恶性肿瘤。多数患者死于诊断后的1〜2年内。肿瘤治疗电场(TTFields)是一个局部区域传递抗有丝分裂的治疗,干扰细胞分裂和细胞器组装。

Neuro Oncol:基于生物标志物和和改良递归分割分析有助于预测胶质母细胞瘤预后

在RTOG 0525试验中,比较剂量密度和标准剂量的temozolomide对胶质母细胞瘤(GBM)的作用。患者死亡风险的峰值在16个月左右,然后缓慢下降。而进展在6个月后显著下降。同时,MGMT基因启动子甲基化和改良递归分割分析(Recursive Partitioning Analysis,RPA)模型分级III时,在头2年有生存优势。在治疗开始6个月时,采用剂量密度方法在

J Clin Oncol:贝伐珠单抗添加到标准治疗对新诊断胶质母细胞瘤的患者生存质量没有影响

目的:随着胶质母细胞瘤的进展,患者经历健康相关的生活质量的下降(HRQoL)。延迟这种下降是重要的治疗目标。在新诊断的胶质母细胞瘤中,贝伐珠单抗添加到放射治疗加替莫唑胺(RT / TMZ)  vs 安慰剂加RT / TMZ(III期AVAglio研究中危险比,0.64;95%置信区间,0.55至0.74;P <&