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婴儿非多形性胶质母细胞瘤脑肿瘤中的巨细胞病毒 DNA。

Cytomegalovirus DNA in non-glioblastoma multiforme brain tumors of infants.

机构信息

Department of Pediatric Neurosurgery, Children's Medical Center Hospital, Tehran University of Medical Sciences, Tehran, Iran.

Department of Pediatric Pathology, Children's Medical Center Hospital, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Childs Nerv Syst. 2021 May;37(5):1581-1586. doi: 10.1007/s00381-021-05038-6. Epub 2021 Jan 7.

Abstract

PURPOSE

CMV antigens have been detected in some brain tumors specially glioblastoma multiforme (GBM). As brain tumors in the first years of life are among the most aggressive neoplasms with poor prognosis, novel therapeutic options like targeted therapy against virus antigens are demanded. Infantile central nervous system tumors, other than GBM, have not been so far studied for CMV. To our best knowledge, this is the first study in which the presence of CMV-DNA, as a potential viral target for therapy, in non-GBM infantile brain tumors has been investigated.

METHODS

The paraffin blocks of non-GBM brain neoplasms of 36 infants (age < 24 months) who were operated on between 2006 and 2016 were examined for CMV-DNA, using real-time polymerase chain reaction (PCR). Paraffin blocks of CMV infected lung tissue were used as positive control. Extraction and amplification of β2 microglobulin gene from each tumor tissue were carried as positive internal control. We also assayed 25 paraffin blocks of meningomyelocele for CMV DNA as negative tissue controls.

RESULTS

Histopathological diagnoses consisted of 13 glial/neuroglial tumors (36.1%), 8 ependymomas (22.2%), 7 medulloblastomas (19.4%), 3 choroid plexus tumors (8.3%), 2 atypical teratoid rhabdoid tumors (5.6%), 2 embryonal CNS tumors (5.6%), and 1 germ cell tumor (2.8%). We could not detect CMV DNA in all samples examined.

CONCLUSION

Although CMV may be associated with GBM, no role could be proposed for this virus in development of non-GBM infantile brain tumors. Further investigations on larger series of brain tumors should be conducted to confirm or rule out our conclusion.

摘要

目的

巨细胞病毒(CMV)抗原已在某些脑瘤中被检测到,特别是多形性胶质母细胞瘤(GBM)。由于儿童期脑肿瘤是侵袭性最强、预后最差的肿瘤之一,因此需要针对病毒抗原的靶向治疗等新的治疗选择。到目前为止,婴儿中枢神经系统肿瘤(除 GBM 外)尚未对此进行 CMV 研究。据我们所知,这是首次研究 CMV-DNA 作为治疗的潜在病毒靶点在非 GBM 婴儿脑肿瘤中的存在情况。

方法

使用实时聚合酶链反应(PCR)对 2006 年至 2016 年间接受手术的 36 名年龄<24 个月的婴儿非 GBM 脑肿瘤的石蜡块进行 CMV-DNA 检测。CMV 感染的肺组织石蜡块作为阳性对照。从每个肿瘤组织中提取和扩增β2 微球蛋白基因作为阳性内对照。我们还对 25 例脑脊膜膨出的石蜡块进行了 CMV DNA 检测作为阴性组织对照。

结果

组织病理学诊断包括 13 例神经胶质/神经胶质瘤(36.1%)、8 例室管膜瘤(22.2%)、7 例髓母细胞瘤(19.4%)、3 例脉络丛肿瘤(8.3%)、2 例非典型畸胎瘤横纹肌样瘤(5.6%)、2 例胚胎性中枢神经系统肿瘤(5.6%)和 1 例生殖细胞瘤(2.8%)。我们未能在所有检测样本中检测到 CMV DNA。

结论

尽管 CMV 可能与 GBM 相关,但不能认为该病毒在非 GBM 婴儿脑肿瘤的发生中起作用。应该对更大系列的脑肿瘤进行进一步研究,以确认或排除我们的结论。

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