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1
The "Spot 14" gene resides on the telomeric end of the 11q13 amplicon and is expressed in lipogenic breast cancers: implications for control of tumor metabolism.“斑点14”基因位于11q13扩增子的端粒末端,在脂肪生成性乳腺癌中表达:对肿瘤代谢控制的意义。
Proc Natl Acad Sci U S A. 1998 Jun 9;95(12):6989-94. doi: 10.1073/pnas.95.12.6989.
2
"Spot 14" protein: a metabolic integrator in normal and neoplastic cells.“斑点14”蛋白:正常细胞和肿瘤细胞中的一种代谢整合蛋白。
Thyroid. 1998 Sep;8(9):815-25. doi: 10.1089/thy.1998.8.815.
3
Modulation of tumor fatty acids, through overexpression or loss of thyroid hormone responsive protein spot 14 is associated with altered growth and metastasis.通过甲状腺激素反应蛋白斑点14的过表达或缺失来调节肿瘤脂肪酸,与生长和转移的改变有关。
Breast Cancer Res. 2014 Dec 4;16(6):481. doi: 10.1186/s13058-014-0481-z.
4
Progestins and androgens increase expression of Spot 14 in T47-D breast tumor cells.孕激素和雄激素可增加T47-D乳腺肿瘤细胞中Spot 14的表达。
Biochem Biophys Res Commun. 2000 Mar 5;269(1):209-12. doi: 10.1006/bbrc.2000.2262.
5
The spot 14 protein inhibits growth and induces differentiation and cell death of human MCF-7 breast cancer cells.斑点14蛋白可抑制人MCF - 7乳腺癌细胞的生长,并诱导其分化和细胞死亡。
Biochem J. 2005 Aug 15;390(Pt 1):57-65. doi: 10.1042/BJ20042080.
6
DNA amplification at 11q13.5-q14 in human breast cancer.人类乳腺癌中11号染色体长臂13.5区至14区的DNA扩增
Oncogene. 1992 Dec;7(12):2513-7.
7
S14 protein in breast cancer cells: direct evidence of regulation by SREBP-1c, superinduction with progestin, and effects on cell growth.乳腺癌细胞中的S14蛋白:SREBP-1c调控的直接证据、孕激素的超诱导作用及其对细胞生长的影响
Exp Cell Res. 2006 Feb 1;312(3):278-88. doi: 10.1016/j.yexcr.2005.10.022. Epub 2005 Nov 21.
8
High-resolution genomic analysis of the 11q13 amplicon in breast cancers identifies synergy with 8p12 amplification, involving the mTOR targets S6K2 and 4EBP1.对乳腺癌中 11q13 扩增子的高分辨率基因组分析鉴定出与 8p12 扩增的协同作用,涉及 mTOR 靶标 S6K2 和 4EBP1。
Genes Chromosomes Cancer. 2011 Oct;50(10):775-87. doi: 10.1002/gcc.20900. Epub 2011 Jul 11.
9
Expression of "Spot 14" (THRSP) predicts disease free survival in invasive breast cancer: immunohistochemical analysis of a new molecular marker.“斑点14”(THRSP)的表达可预测浸润性乳腺癌的无病生存期:一种新分子标志物的免疫组化分析
Breast Cancer Res Treat. 2006 Jul;98(2):231-40. doi: 10.1007/s10549-005-9154-z. Epub 2006 Mar 22.
10
Amplification of the BRCA2 pathway gene EMSY in sporadic breast cancer is related to negative outcome.散发性乳腺癌中BRCA2通路基因EMSY的扩增与不良预后相关。
Clin Cancer Res. 2004 Sep 1;10(17):5785-91. doi: 10.1158/1078-0432.CCR-03-0410.

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1
Lipid metabolism dynamics in cancer stem cells: potential targets for cancers.癌症干细胞中的脂质代谢动态:癌症的潜在靶点。
Front Pharmacol. 2024 Jun 27;15:1367981. doi: 10.3389/fphar.2024.1367981. eCollection 2024.
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Lipid metabolism alteration contributes to and maintains the properties of cancer stem cells.脂质代谢改变有助于并维持癌症干细胞的特性。
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The serum level of a novel lipogenic protein Spot 14 was reduced in metabolic syndrome.新型脂肪生成蛋白 Spot 14 的血清水平在代谢综合征中降低。
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5
When fats commit crimes: fatty acid metabolism, cancer stemness and therapeutic resistance.当脂肪犯罪时:脂肪酸代谢、癌症干性和治疗抵抗。
Cancer Commun (Lond). 2018 Jul 11;38(1):47. doi: 10.1186/s40880-018-0317-9.
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Ammonium tetrathiomolybdate treatment targets the copper transporter ATP7A and enhances sensitivity of breast cancer to cisplatin.四硫代钼酸铵治疗靶向铜转运蛋白ATP7A并增强乳腺癌对顺铂的敏感性。
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Sebaceous Gland Atrophy in Psoriasis: An Explanation for Psoriatic Alopecia?银屑病中的皮脂腺萎缩:银屑病性脱发的一种解释?
J Invest Dermatol. 2016 Sep;136(9):1792-1800. doi: 10.1016/j.jid.2016.05.113. Epub 2016 Jun 14.
8
Fatty Acids and Breast Cancer: Make Them on Site or Have Them Delivered.脂肪酸与乳腺癌:原位生成还是外源性供给。
J Cell Physiol. 2016 Oct;231(10):2128-41. doi: 10.1002/jcp.25332. Epub 2016 Feb 16.
9
Obesity and cancer progression: is there a role of fatty acid metabolism?肥胖与癌症进展:脂肪酸代谢是否起作用?
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10
Modulation of tumor fatty acids, through overexpression or loss of thyroid hormone responsive protein spot 14 is associated with altered growth and metastasis.通过甲状腺激素反应蛋白斑点14的过表达或缺失来调节肿瘤脂肪酸,与生长和转移的改变有关。
Breast Cancer Res. 2014 Dec 4;16(6):481. doi: 10.1186/s13058-014-0481-z.

本文引用的文献

1
Spot 14 protein-protein interactions: evidence for both homo- and heterodimer formation in vivo.斑点14蛋白-蛋白相互作用:体内同源和异源二聚体形成的证据。
Endocrinology. 1997 Dec;138(12):5184-8. doi: 10.1210/endo.138.12.5597.
2
EMS1 amplification can occur independently of CCND1 or INT-2 amplification at 11q13 and may identify different phenotypes in primary breast cancer.EMS1扩增可独立于11q13处的CCND1或INT-2扩增而发生,并且可能在原发性乳腺癌中识别出不同的表型。
Oncogene. 1997 Sep 25;15(13):1617-23. doi: 10.1038/sj.onc.1201311.
3
Assignment of the "spot 14" gene (THRSP) to human chromosome band 11q13.5 by in situ hybridization.通过原位杂交将“斑点14”基因(THRSP)定位于人类染色体11q13.5带。
Cytogenet Cell Genet. 1997;78(2):131-2. doi: 10.1159/000134644.
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The human uncoupling protein-3 gene. Genomic structure, chromosomal localization, and genetic basis for short and long form transcripts.人类解偶联蛋白-3基因。基因组结构、染色体定位以及长短转录本的遗传基础。
J Biol Chem. 1997 Oct 10;272(41):25433-6. doi: 10.1074/jbc.272.41.25433.
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Assignment of acetyl-CoA carboxylase-beta (ACACB) to human chromosome band 12q24.1 by in situ hybridization.
Cytogenet Cell Genet. 1997;77(3-4):176-7. doi: 10.1159/000134568.
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Increased expression of fatty acid synthase (OA-519) in ovarian neoplasms predicts shorter survival.
Hum Pathol. 1997 Jun;28(6):686-92. doi: 10.1016/s0046-8177(97)90177-5.
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Assignment of thyroid hormone responsive SPOT 14 homolog (THRSP) to human chromosome 11 bands q13.5-->q14.1 by in situ hybridization.通过原位杂交将甲状腺激素反应性SPOT 14同源物(THRSP)定位到人类染色体11的q13.5→q14.1区域。
Cytogenet Cell Genet. 1997;76(3-4):219-20. doi: 10.1159/000134553.
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A 5.5-Mb high-resolution integrated map of distal 11q13.
Genomics. 1997 Feb 1;39(3):340-7. doi: 10.1006/geno.1996.4460.
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The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A).1型Usher综合征(MYO7A)缺陷基因的基因组结构
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Framework YAC contig anchored into a 3.2-Mb high-resolution physical map in proximal 11q13.框架酵母人工染色体(YAC)重叠群定位于11号染色体长臂近端13区3.2兆碱基的高分辨率物理图谱中。
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“斑点14”基因位于11q13扩增子的端粒末端,在脂肪生成性乳腺癌中表达:对肿瘤代谢控制的意义。

The "Spot 14" gene resides on the telomeric end of the 11q13 amplicon and is expressed in lipogenic breast cancers: implications for control of tumor metabolism.

作者信息

Moncur J T, Park J P, Memoli V A, Mohandas T K, Kinlaw W B

机构信息

Dartmouth Medical School, 1 Medical Center Drive, Lebanon, NH 03756, USA.

出版信息

Proc Natl Acad Sci U S A. 1998 Jun 9;95(12):6989-94. doi: 10.1073/pnas.95.12.6989.

DOI:10.1073/pnas.95.12.6989
PMID:9618526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC22712/
Abstract

Enhanced long chain fatty acid synthesis may occur in breast cancer, where it is necessary for tumor growth and predicts a poor prognosis. "Spot 14" (S14) is a carbohydrate- and thyroid hormone-inducible nuclear protein specific to liver, adipose, and lactating mammary tissues that functions to activate genes encoding the enzymes of fatty acid synthesis. Amplification of chromosome region 11q13, where the S14 gene (THRSP) resides, also predicts a poor prognosis in breast tumors. We localized the S14 gene between markers D11S906 and D11S937, at the telomeric end of the amplified region at 11q13, and found that it was amplified and expressed in breast cancer-derived cell lines. Moreover, concordant expression of S14 and a key lipogenic enzyme (acetyl-CoA carboxylase) in a panel of primary breast cancer specimens strongly supported a role for S14 as a determinant of tumor lipid metabolism. S14 expression provides a pathophysiological link between two prognostic indicators in breast cancer: enhanced lipogenesis and 11q13 amplification.

摘要

在乳腺癌中可能会出现长链脂肪酸合成增强的情况,这对肿瘤生长至关重要且预示着预后不良。“斑点14”(S14)是一种碳水化合物和甲状腺激素诱导的核蛋白,特异性存在于肝脏、脂肪组织和泌乳乳腺组织中,其功能是激活编码脂肪酸合成酶的基因。11号染色体区域11q13(S14基因(THRSP)所在区域)的扩增也预示着乳腺肿瘤预后不良。我们将S14基因定位在标记D11S906和D11S937之间,位于11q13扩增区域的端粒末端,并发现它在乳腺癌衍生的细胞系中扩增且表达。此外,在一组原发性乳腺癌标本中,S14和一种关键的脂肪生成酶(乙酰辅酶A羧化酶)的协同表达有力地支持了S14作为肿瘤脂质代谢决定因素的作用。S14表达在乳腺癌的两个预后指标之间提供了一个病理生理联系:脂肪生成增强和11q13扩增。