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小儿肉瘤

Pediatric sarcomas.

作者信息

Cao Junhua, An Qi, Wang Lei

机构信息

Department of Pediatric Internal Medicine, Xuzhou Children's Hospital, Xuzhou, Jiangsu 221002, P.R. China.

出版信息

Oncol Lett. 2018 Feb;15(2):1397-1402. doi: 10.3892/ol.2017.7467. Epub 2017 Nov 21.

DOI:10.3892/ol.2017.7467
PMID:29434830
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5776166/
Abstract

Sarcomas arise from primitive mesenchymal cells, which are classified, into two main groups: Bone and soft tissue sarcomas. We have searched all-important electronic databases including Google scholar and PubMed for the collection of latest literature pertaining to pediatric sarcomas. Latest literature confirmed that these tumors are relatively rare and represent only 1% of all malignancies but they have higher incidence in children. Pediatric sarcomas comprise about 13% of all pediatric malignancies and are ranked third in childhood cancers. The highest incidence rates are reported among rhabdomyosarcoma, osteosarcoma and Ewing's sarcomas in children. All of these neoplasms often display highly aggressive behavior with tendency to form metastases. Important globally used management avenues include surgery with systemic chemotherapy and have success rate of 70% at 5-years. Furthermore, in the cases of advanced stages, the prognosis is poor, chances of treatment failure and recurrence are quite high. Utilization of cancer stem cells is the latest approach with great potential in management of above pathological state. The present review article discuss all-important aspects of commonly found pediatric sarcomas throughout the world.

摘要

肉瘤起源于原始间充质细胞,可分为两大类:骨肉瘤和软组织肉瘤。我们检索了所有重要的电子数据库,包括谷歌学术和PubMed,以收集有关小儿肉瘤的最新文献。最新文献证实,这些肿瘤相对罕见,仅占所有恶性肿瘤的1%,但在儿童中的发病率较高。小儿肉瘤约占所有小儿恶性肿瘤的13%,在儿童癌症中排名第三。据报道,儿童横纹肌肉瘤、骨肉瘤和尤因肉瘤的发病率最高。所有这些肿瘤通常表现出高度侵袭性的行为,并有形成转移的倾向。全球常用的重要治疗方法包括手术加全身化疗,5年成功率为70%。此外,在晚期病例中,预后较差,治疗失败和复发的几率相当高。利用癌症干细胞是治疗上述病理状态的最新方法,具有很大的潜力。本综述文章讨论了全球常见的小儿肉瘤的所有重要方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e06f/5776166/0e678181aa91/ol-15-02-1397-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e06f/5776166/bd5f8e061eff/ol-15-02-1397-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e06f/5776166/cbff50824cd8/ol-15-02-1397-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e06f/5776166/0e678181aa91/ol-15-02-1397-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e06f/5776166/bd5f8e061eff/ol-15-02-1397-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e06f/5776166/cbff50824cd8/ol-15-02-1397-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e06f/5776166/0e678181aa91/ol-15-02-1397-g02.jpg

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1
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2
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[Clinical patterns of soft-tissue sarcoma in children].[儿童软组织肉瘤的临床模式]
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引用本文的文献

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Preclinical In Vivo Modeling of Pediatric Sarcoma-Promises and Limitations.小儿肉瘤的临床前体内建模:前景与局限
J Clin Med. 2021 Apr 8;10(8):1578. doi: 10.3390/jcm10081578.
2
[Twist regulates proliferation, migration and invasion of osteosarcoma cells in vitro].[Twist调节骨肉瘤细胞在体外的增殖、迁移和侵袭]
Nan Fang Yi Ke Da Xue Xue Bao. 2018 May 20;38(5):554-560. doi: 10.3969/j.issn.1673-4254.2018.05.08.

本文引用的文献

1
Soft tissue sarcomas in adolescents and young adults: a comparison with their paediatric and adult counterparts.青少年和年轻成人的软组织肉瘤:与儿科和成人患者的比较。
Lancet Oncol. 2017 Mar;18(3):e166-e175. doi: 10.1016/S1470-2045(17)30099-2. Epub 2017 Mar 2.
2
Novel insights and therapeutic interventions for pediatric osteosarcoma.小儿骨肉瘤的新见解与治疗干预措施
Future Oncol. 2017 Feb;13(4):357-368. doi: 10.2217/fon-2016-0261. Epub 2016 Sep 21.
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Prognostic value of cancer stem cell marker CD133 expression in pancreatic ductal adenocarcinoma (PDAC): a systematic review and meta-analysis.
癌症干细胞标志物CD133表达在胰腺导管腺癌(PDAC)中的预后价值:一项系统评价和荟萃分析
Int J Clin Exp Pathol. 2015 Oct 1;8(10):12084-92. eCollection 2015.
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Chemotherapy induces stemness in osteosarcoma cells through activation of Wnt/β-catenin signaling.化疗通过激活 Wnt/β-catenin 信号通路诱导骨肉瘤细胞干性。
Cancer Lett. 2016 Jan 28;370(2):286-95. doi: 10.1016/j.canlet.2015.11.013. Epub 2015 Nov 11.
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Aldehyde Dehydrogenase 1B1 as a Modulator of Pancreatic Adenocarcinoma.乙醛脱氢酶1B1作为胰腺腺癌的调节剂
Pancreas. 2016 Jan;45(1):117-22. doi: 10.1097/MPA.0000000000000542.
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Brief Report: Inhibition of miR-145 Enhances Reprogramming of Human Dermal Fibroblasts to Induced Pluripotent Stem Cells.简短报告:miR-145的抑制增强人皮肤成纤维细胞重编程为诱导多能干细胞的过程。
Stem Cells. 2016 Jan;34(1):246-51. doi: 10.1002/stem.2220. Epub 2015 Oct 9.
7
Osteosarcoma Stem Cells Have Active Wnt/β-catenin and Overexpress SOX2 and KLF4.骨肉瘤干细胞具有活跃的Wnt/β-连环蛋白信号通路,且SOX2和KLF4表达上调。
J Cell Physiol. 2016 Apr;231(4):876-86. doi: 10.1002/jcp.25179. Epub 2015 Sep 9.
8
Identification of Discrete Prognostic Groups in Ewing Sarcoma.尤因肉瘤中离散预后组的鉴定
Pediatr Blood Cancer. 2016 Jan;63(1):47-53. doi: 10.1002/pbc.25709. Epub 2015 Aug 10.
9
CXCR4--A Prognostic and Clinicopathological Biomarker for Pancreatic Ductal Adenocarcinoma: A Meta-Analysis.CXCR4——胰腺导管腺癌的一种预后及临床病理生物标志物:一项荟萃分析
PLoS One. 2015 Jun 19;10(6):e0130192. doi: 10.1371/journal.pone.0130192. eCollection 2015.
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Aldehyde Dehydrogenase 1 (ALDH1) Is a Potential Marker for Cancer Stem Cells in Embryonal Rhabdomyosarcoma.醛脱氢酶1(ALDH1)是胚胎性横纹肌肉瘤中癌症干细胞的潜在标志物。
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