Suppr超能文献

羧肽酶 E:在嗜铬细胞瘤和其他癌症中表达升高与肿瘤生长和转移相关。

Carboxypeptidase E: elevated expression correlated with tumor growth and metastasis in pheochromocytomas and other cancers.

机构信息

Section on Cellular Neurobiology, Program on Developmental Neuroscience, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bldg. 49, Rm. 5A22, 49 Convent Drive, MSC 4480, Bethesda, MD 20892, USA.

出版信息

Cell Mol Neurobiol. 2010 Nov;30(8):1377-81. doi: 10.1007/s10571-010-9592-y.

Abstract

Expression of carboxypeptidase E (CPE), a prohormone processing enzyme in different cancer types, was analyzed from data in the GEO profile database (http://www.ncbi.nlm.nih.gov/geo/) and experimentally in pheochromocytomas. Analysis of microarray data demonstrated that significantly elevated levels of CPE mRNA was found in many metastatic non-endocrine cancers: cervical, colon rectal, renal cancers, Ewing sarcomas (bone cancer), and various types of astrocytomas and oligodendrogliomas, whereas expression of CPE mRNA was virtually absent in their respective counterpart normal tissues. Moreover, there was higher CPE mRNA expression in cells from the metastatic tumor compared to those from the primary tumor in colorectal cancer. Elevated CPE mRNA expression was found in neuroendocrine tumors in lung and pituitary adenomas, although the significance is unclear since endocrine and neuroendocrine cells normally express CPE. However, studies of neuroendocrine tumors, pheochromocytomas, revealed expression of not only wild-type CPE, but a variant which was correlated with tumor behavior. Extremely high CPE mRNA copy numbers of the variant were found in very large or invasive tumors, both of which usually indicate poor prognosis. Thus, collectively the data suggest that CPE may play a role in promoting tumor growth and invasion. CPE could potentially serve as a diagnostic and prognostic biomarker for metastasis in different cancer types.

摘要

羧肽酶 E(CPE)是一种前激素加工酶,其在不同癌症类型中的表达,是从 GEO 数据库(http://www.ncbi.nlm.nih.gov/geo/)中的数据进行分析,并在嗜铬细胞瘤中进行实验得出的。微阵列数据分析表明,在许多转移性非内分泌癌症中,CPE mRNA 的水平显著升高:宫颈癌、结直肠癌、肾癌、尤因肉瘤(骨癌)和各种类型的星形细胞瘤和少突胶质细胞瘤,而在相应的正常组织中几乎没有 CPE mRNA 的表达。此外,在结直肠癌中,转移性肿瘤细胞中的 CPE mRNA 表达高于原发性肿瘤细胞。在肺和垂体腺瘤中的神经内分泌肿瘤中也发现了 CPE mRNA 的高表达,尽管由于内分泌和神经内分泌细胞通常表达 CPE,因此其意义尚不清楚。然而,对神经内分泌肿瘤、嗜铬细胞瘤的研究表明,不仅表达了野生型 CPE,还表达了与肿瘤行为相关的变异型。在体积非常大或侵袭性的肿瘤中发现了极高的 CPE mRNA 变异型拷贝数,这两者通常都预示着预后不良。因此,这些数据表明 CPE 可能在促进肿瘤生长和侵袭中发挥作用。CPE 可能成为不同癌症类型转移的诊断和预后生物标志物。

相似文献

3
Carboxypeptidase E and its splice variants: Key regulators of growth and metastasis in multiple cancer types.
Cancer Lett. 2022 Nov 1;548:215882. doi: 10.1016/j.canlet.2022.215882. Epub 2022 Aug 18.
4
Overexpression of CPE-ΔN predicts poor prognosis in colorectal cancer patients.
Tumour Biol. 2013 Dec;34(6):3691-9. doi: 10.1007/s13277-013-0952-3. Epub 2013 Jul 14.
5
CPE overexpression is correlated with pelvic lymph node metastasis and poor prognosis in patients with early-stage cervical cancer.
Arch Gynecol Obstet. 2016 Aug;294(2):333-42. doi: 10.1007/s00404-015-3985-6. Epub 2015 Dec 22.
8
Silencing of Carboxypeptidase E expression inhibits proliferation and invasion of Panc-1 pancreatic cancer cells.
F1000Res. 2021 Jun 22;10:489. doi: 10.12688/f1000research.53737.2. eCollection 2021.
10

引用本文的文献

3
N-terminal truncated carboxypeptidase E expression is associated with poor prognosis of lung adenocarcinoma.
Oncol Lett. 2016 Dec;12(6):4659-4664. doi: 10.3892/ol.2016.5283. Epub 2016 Oct 18.
5
Silencing of carboxypeptidase E inhibits cell proliferation, tumorigenicity, and metastasis of osteosarcoma cells.
Onco Targets Ther. 2016 May 10;9:2795-803. doi: 10.2147/OTT.S98991. eCollection 2016.
6
Carboxypeptidase E is a prediction marker for tumor recurrence in early-stage hepatocellular carcinoma.
Tumour Biol. 2016 Jul;37(7):9745-53. doi: 10.1007/s13277-016-4814-7. Epub 2016 Jan 23.
8
18F-FLT PET/CT in the Evaluation of Pheochromocytomas and Paragangliomas: A Pilot Study.
J Nucl Med. 2015 Dec;56(12):1849-54. doi: 10.2967/jnumed.115.159061. Epub 2015 Sep 10.
9
[Screening of Highly Expressed CPEΔN Lung Cancer H1299 Cells].
Zhongguo Fei Ai Za Zhi. 2015 Jun;18(6):340-4. doi: 10.3779/j.issn.1009-3419.2015.06.03.
10
Target therapy in metastatic pheochromocytoma: current perspectives and controversies.
Oncol Rev. 2014 Sep 23;8(2):249. doi: 10.4081/oncol.2014.249.

本文引用的文献

1
Obese carboxypeptidase E knockout mice exhibit multiple defects in peptide hormone processing contributing to low bone mineral density.
Am J Physiol Endocrinol Metab. 2010 Aug;299(2):E189-97. doi: 10.1152/ajpendo.00516.2009. Epub 2010 May 11.
3
PC2/CPE-mediated pro-protein processing in tumor cells and its differentiated cells or tissues.
Mol Cell Endocrinol. 2009 May 6;303(1-2):43-9. doi: 10.1016/j.mce.2009.01.020. Epub 2009 Feb 7.
4
A bi-directional carboxypeptidase E-driven transport mechanism controls BDNF vesicle homeostasis in hippocampal neurons.
Mol Cell Neurosci. 2008 Sep;39(1):63-73. doi: 10.1016/j.mcn.2008.05.016. Epub 2008 Jun 4.
5
Detection of a microRNA signal in an in vivo expression set of mRNAs.
PLoS One. 2007 Aug 29;2(8):e804. doi: 10.1371/journal.pone.0000804.
7
Pheochromocytoma: recommendations for clinical practice from the First International Symposium. October 2005.
Nat Clin Pract Endocrinol Metab. 2007 Feb;3(2):92-102. doi: 10.1038/ncpendmet0396.
8
Gene expression profiling in cervical cancer: an exploration of intratumor heterogeneity.
Clin Cancer Res. 2006 Oct 1;12(19):5632-40. doi: 10.1158/1078-0432.CCR-06-0357.
9
Global alterations in mRNA polysomal recruitment in a cell model of colorectal cancer progression to metastasis.
Carcinogenesis. 2006 Jul;27(7):1323-33. doi: 10.1093/carcin/bgi377. Epub 2006 Mar 10.
10

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验