"Neoplasm Proteins" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Proteins whose abnormal expression (gain or loss) are associated with the development, growth, or progression of NEOPLASMS. Some neoplasm proteins are tumor antigens (ANTIGENS, NEOPLASM), i.e. they induce an immune reaction to their tumor. Many neoplasm proteins have been characterized and are used as tumor markers (BIOMARKERS, TUMOR) when they are detectable in cells and body fluids as monitors for the presence or growth of tumors. Abnormal expression of ONCOGENE PROTEINS is involved in neoplastic transformation, whereas the loss of expression of TUMOR SUPPRESSOR PROTEINS is involved with the loss of growth control and progression of the neoplasm.
Descriptor ID |
D009363
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MeSH Number(s) |
D12.776.624
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Neoplasm Proteins".
Below are MeSH descriptors whose meaning is more specific than "Neoplasm Proteins".
This graph shows the total number of publications written about "Neoplasm Proteins" by people in this website by year, and whether "Neoplasm Proteins" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1995 | 3 | 3 | 6 |
1996 | 5 | 2 | 7 |
1997 | 4 | 2 | 6 |
1998 | 9 | 1 | 10 |
1999 | 5 | 2 | 7 |
2000 | 6 | 0 | 6 |
2001 | 3 | 2 | 5 |
2002 | 1 | 1 | 2 |
2003 | 6 | 3 | 9 |
2004 | 8 | 8 | 16 |
2005 | 10 | 2 | 12 |
2006 | 6 | 4 | 10 |
2007 | 4 | 6 | 10 |
2008 | 8 | 8 | 16 |
2009 | 3 | 2 | 5 |
2010 | 2 | 2 | 4 |
2011 | 5 | 3 | 8 |
2012 | 3 | 6 | 9 |
2013 | 6 | 3 | 9 |
2014 | 5 | 5 | 10 |
2015 | 16 | 1 | 17 |
2016 | 6 | 0 | 6 |
2017 | 5 | 2 | 7 |
2018 | 9 | 0 | 9 |
2019 | 3 | 1 | 4 |
2020 | 1 | 2 | 3 |
2021 | 1 | 0 | 1 |
2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Neoplasm Proteins" by people in Profiles.
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Primary Spindle Cell Sarcoma of the Lung with MGA::NUTM1 Fusion: An Extremely Rare Case of a Potentially Emerging Entity and Review of the Literature. Int J Surg Pathol. 2022 Dec; 30(8):931-938.
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The Roles of Post-Translational Modifications on mTOR Signaling. Int J Mol Sci. 2021 Feb 11; 22(4).
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Bioactive sphingolipids: Advancements and contributions from the laboratory of Dr. Lina M. Obeid. Cell Signal. 2021 03; 79:109875.
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Zonal regulation of collagen-type proteins and posttranslational modifications in prostatic benign and cancer tissues by imaging mass spectrometry. Prostate. 2020 09; 80(13):1071-1086.
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Discovery of proangiogenic CD44+mesenchymal cancer stem cells in an acute myeloid leukemia patient's bone marrow. J Hematol Oncol. 2020 06 03; 13(1):63.
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Identification of novel epithelial ovarian cancer loci in women of African ancestry. Int J Cancer. 2020 06 01; 146(11):2987-2998.
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SLC36A1-mTORC1 signaling drives acquired resistance to CDK4/6 inhibitors. Sci Adv. 2019 09; 5(9):eaax6352.
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Intraductal Adaptation of the 4T1 Mouse Model of Breast Cancer Reveals Effects of the Epithelial Microenvironment on Tumor Progression and Metastasis. Anticancer Res. 2019 May; 39(5):2277-2287.
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TGF? promotes breast cancer stem cell self-renewal through an ILEI/LIFR signaling axis. Oncogene. 2019 05; 38(20):3794-3811.
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Inhibition of de novo lipogenesis targets androgen receptor signaling in castration-resistant prostate cancer. Proc Natl Acad Sci U S A. 2019 01 08; 116(2):631-640.