Evidence map›Paper›PMID 18183490›Full record

ArticlePituitary2008

Molecular pathogenesis of human prolactinomas identified by gene expression profiling, RT-qPCR, and proteomic analyses.

Chheng-Orn Evans, Carlos S Moreno, Xianquan Zhan, Michael T McCabe, Paula M Vertino, Dominic M Desiderio, Nelson M Oyesiku

Abstract read
PubMed Publisher
In one paragraph

Article in Pituitary, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 88 citations in OpenAlex.

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  17. Review
  18. The Epigenomics of Pituitary Adenoma.Frontiers in endocrinology · 2019
    Review
  19. Proteomic Analysis of the Human Anterior Pituitary Gland.Omics : a journal of integrative biology · 2018
    Article
  20. Human Prolactinoma: A View of Protein-Protein Interaction Pattern.International journal of endocrinology and metabolism · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Chheng-Orn EvansDepartment of Neurosurgery and Laboratory of Molecular Neurosurgery and Biotechnology, Emory University School of Medicine, 1365 B Clifton Rd., NE, Suite. 6200, Atlanta, GA, 30322, USA.
Carlos S Moreno
Xianquan Zhan
Michael T McCabe
Paula M Vertino
Dominic M Desiderio
Nelson M Oyesiku
Emory University · USUniversity of Tennessee at Knoxville · USUniversity of Tennessee Health Science Center · US

Funding

GENESIS AND CONSEQUENCES OF ABERRANT DNA METHYLATIONR01CA077337 · NCI · EMORY UNIVERSITY · PI VERTINO, PAULA M. · 1998 to 2016
$3.4M
Developmental Transcription Factors in Prostate CancerR01CA106826 · NCI · EMORY UNIVERSITY · PI MORENO, CARLOS SANCHEZ · 2005 to 2013
$2.6M
ANALYSIS OF THE PROTEOME IN HUMAN PITUITARY TUMORSR01NS042843 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI DESIDERIO, DOMINIC M · 2001 to 2005
$1.5M
Quality Threshold Analysis of Prostate CancersK22CA096560 · NCI · EMORY UNIVERSITY · PI MORENO, CARLOS S · 2002 to 2004
$453k
LC-ELECTROSPRAY QUADRUPOLE ION TRAP MASS SPECTROMETERS10RR014593 · NCRR · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI DESIDERIO, DOMINIC M · 2000 to 2000
$243k
MALDI TOF MASS SPECTROMETERS10RR010522 · NCRR · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI DESIDERIO, DOMINIC M · 1997 to 1997
–
NCI NIH HHS 2R01-CA077337NCI NIH HHS K22-CA96560NCI NIH HHS R01-CA106826NCRR NIH HHS RR-10522NCRR NIH HHS RR-14593NINDS NIH HHS NS 42843
6 · The paper itself

Abstract

The molecular pathogenesis of prolactinomas has resisted elucidation; with the exception of a RAS mutation in a single aggressive prolactinoma, no mutational changes have been identified. In prolactinomas, a further obstacle has been the paucity of surgical specimens suitable for molecular analysis since prolactionomas are infrequently removed due to the availability and effectiveness of medical therapy. In the absence of mutational events, gene expression changes have been sought and detected. Using high-throughput analysis from a large bank of human pituitary adenomas, we examined these tumors according to their molecular profiles rather than traditional immunohistochemistry. We examined six prolactinomas and eight normal pituitary glands using oligonucleotide GeneChip microarrays, reverse transcription-real time quantitative polymerase chain reaction using 10 prolactinomas, and proteomic analysis to examine protein expression in four prolactinomas. Microarray analyses identified 726 unique genes that were statistically significantly different between prolactinomas and normal glands, whereas proteomic analysis identified four differently up-regulated and 19 down-regulated proteins. Several components of the Notch pathway were altered in prolactinomas, and there was an increased expression of the Pit-1 transcription factor, and the survival factor BAG1 but decreased E-cadherin and N-cadherin expression. Taken together, expression profiling and proteomic analyses have identified molecular features unique to prolactinomas that may contribute to their pathogenesis. In the current era of molecular medicine, these findings greatly enhance our understanding and supercede immunohistochemical diagnosis.

Indexed as

Gene Expression ProfilingMolecular Diagnostic TechniquesOligonucleotide Array Sequence AnalysisProteomicsReverse Transcriptase Polymerase Chain ReactionAdenomaAdultCluster AnalysisDNA, NeoplasmFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNeoplasm ProteinsPituitary NeoplasmsDNA, NeoplasmNeoplasm ProteinsRNA, Neoplasm

Identifiers

PMID18183490
OpenAlexW2052731809

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.