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本文引用的文献

1
Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays.使用高密度单核苷酸多态性阵列对黑色素瘤进行全基因组杂合性缺失和拷贝数分析。
Cancer Res. 2007 Mar 15;67(6):2632-42. doi: 10.1158/0008-5472.CAN-06-4152.
2
Genome-wide allelic imbalance analysis of pediatric gliomas by single nucleotide polymorphic allele array.利用单核苷酸多态性等位基因阵列对儿童胶质瘤进行全基因组等位基因失衡分析。
Cancer Res. 2006 Dec 1;66(23):11172-8. doi: 10.1158/0008-5472.CAN-06-2438.
3
Evaluation of S100A10, annexin II and B-FABP expression as markers for renal cell carcinoma.评估S100A10、膜联蛋白II和B-FABP表达作为肾细胞癌标志物的情况。
Cancer Sci. 2007 Jan;98(1):77-82. doi: 10.1111/j.1349-7006.2006.00355.x.
4
Sentinel-node biopsy or nodal observation in melanoma.黑色素瘤的前哨淋巴结活检或淋巴结观察
N Engl J Med. 2006 Sep 28;355(13):1307-17. doi: 10.1056/NEJMoa060992.
5
The prognostic value of circulating tumor cells in patients with melanoma: a systematic review and meta-analysis.循环肿瘤细胞在黑色素瘤患者中的预后价值:一项系统评价和荟萃分析
Clin Cancer Res. 2006 Aug 1;12(15):4605-13. doi: 10.1158/1078-0432.CCR-06-0823.
6
A new melanoma antigen fatty acid-binding protein 7, involved in proliferation and invasion, is a potential target for immunotherapy and molecular target therapy.一种参与增殖和侵袭的新型黑色素瘤抗原脂肪酸结合蛋白7,是免疫治疗和分子靶向治疗的潜在靶点。
Cancer Res. 2006 Apr 15;66(8):4443-9. doi: 10.1158/0008-5472.CAN-05-2505.
7
Microphthalmia transcription factor as a molecular marker for circulating tumor cell detection in blood of melanoma patients.小眼畸形转录因子作为黑色素瘤患者血液中循环肿瘤细胞检测的分子标志物。
Clin Cancer Res. 2006 Feb 15;12(4):1137-43. doi: 10.1158/1078-0432.CCR-05-1847.
8
The clinical significance of MAGEA3 expression in pancreatic cancer.MAGEA3表达在胰腺癌中的临床意义。
Int J Cancer. 2006 May 1;118(9):2269-75. doi: 10.1002/ijc.21656.
9
Serial monitoring of circulating melanoma cells during neoadjuvant biochemotherapy for stage III melanoma: outcome prediction in a multicenter trial.III期黑色素瘤新辅助生物化疗期间循环黑色素瘤细胞的连续监测:一项多中心试验中的结局预测
J Clin Oncol. 2005 Nov 1;23(31):8057-64. doi: 10.1200/JCO.2005.02.0958.
10
Role of Fabp7, a downstream gene of Pax6, in the maintenance of neuroepithelial cells during early embryonic development of the rat cortex.脂肪酸结合蛋白7(Fabp7)作为Pax6的下游基因,在大鼠皮质早期胚胎发育过程中对神经上皮细胞维持的作用。
J Neurosci. 2005 Oct 19;25(42):9752-61. doi: 10.1523/JNEUROSCI.2512-05.2005.

皮肤恶性黑色素瘤中异常的脂肪酸结合蛋白-7 基因表达。

Aberrant fatty acid-binding protein-7 gene expression in cutaneous malignant melanoma.

机构信息

Department of Molecular Oncology, John Wayne Cancer Institute, Santa Monica, California, USA.

出版信息

J Invest Dermatol. 2010 Jan;130(1):221-9. doi: 10.1038/jid.2009.195.

DOI:10.1038/jid.2009.195
PMID:19587692
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2845961/
Abstract

Fatty acid-binding protein-7 (FABP7) has been shown to be expressed in cutaneous melanoma; however, its role in tumor progression is unclear. Expression of FABP7 was assessed during melanoma progression through assessment of various clinicopathology stages of primary tumor progression and metastasis. FABP7 mRNA was highly expressed in 60 of 87 (69%) primary melanomas, compared with significant (P<0.0001) reduction in 13 of 68 (19%) metastatic melanomas. Analysis of 37 paired primary and metastatic melanomas by immunohistochemistry with anti-FABP7 Ab showed 73 and 27% positivity, respectively (P<0.001). FABP7 detection of metastatic tissues was inversely correlated with relapse-free (P<0.0001) and overall (P<0.0001) survival. To examine FABP7 expression loss in advanced melanomas, loss of heterozygosity (LOH) was assessed using microsatellite markers encompassing the FABP7 gene. LOH was identified in 10 of 20 (50%) metastatic melanomas at 6q22.31, compared with 0 of 14 primary melanomas (P=0.0017). FABP7 as a surrogate biomarker for circulating tumor cells (CTCs) in the blood was assessed by quantitative real-time (qRT)-PCR from melanoma patients' blood (n=134). Assessment of patients' blood showed that FABP7(+) CTC decreased with disease progression. FABP7 may function as a tumor progression gene and can be used as a potential diagnostic biomarker of early-stage melanoma systemic spreading in blood.

摘要

脂肪酸结合蛋白 7(FABP7)已被证实存在于皮肤黑色素瘤中;然而,其在肿瘤进展中的作用尚不清楚。通过评估原发性肿瘤进展和转移的各种临床病理阶段,评估 FABP7 在黑色素瘤进展过程中的表达。与 68 例转移性黑色素瘤中的 13 例(19%)相比,60 例 87 例(69%)原发性黑色素瘤中 FABP7 mRNA 表达高度上调。对 37 对原发性和转移性黑色素瘤进行免疫组织化学分析,用抗 FABP7 Ab 显示分别为 73%和 27%阳性(P<0.001)。转移性组织中 FABP7 的检测与无复发生存(P<0.0001)和总生存(P<0.0001)呈负相关。为了研究晚期黑色素瘤中 FABP7 表达缺失,使用微卫星标记物评估 FABP7 基因的杂合性缺失(LOH)。在 20 例转移性黑色素瘤中的 10 例(50%)中鉴定出 6q22.31 的 LOH,而在 14 例原发性黑色素瘤中无 1 例(P=0.0017)。通过定量实时(qRT)-PCR 从黑色素瘤患者的血液(n=134)中评估 FABP7 作为血液中循环肿瘤细胞(CTC)的替代生物标志物。对患者血液的评估表明,FABP7(+)CTC 随疾病进展而减少。FABP7 可能作为肿瘤进展基因发挥作用,并可作为血液中早期黑色素瘤全身性扩散的潜在诊断生物标志物。