Evidence map›Paper›PMID 25841305›Full record

ArticleHuman pathology2015

Transgelin: a potentially useful diagnostic marker differentially expressed in triple-negative and non-triple-negative breast cancers.

Deepthi Rao, Bruce F Kimler, Warren B Nothnick, Marilyn K Davis, Fang Fan, Ossama Tawfik

Abstract read
In one paragraph

Article in Human pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 24% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Biomarkers of tumor invasiveness in proteomics (Review).International journal of oncology · 2020
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
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  8. Article
  9. Review
  10. Article
  11. OncogenicOncotarget · 2018
    Article
  12. Article
  13. Article
  14. Neuron navigator-2 and cyclin D2 are new candidate prognostic markers in uterine sarcoma.Virchows Archiv : an international journal of pathology · 2017
    Article
  15. Article
  16. Article
  17. Expression of Cofilin-1 and Transgelin in Esophageal Squamous Cell Carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2015
    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

6 authors at 2 institutions in 1 country.

Deepthi RaoDepartment of Pathology and Laboratory Medicine, Kansas University Medical Center, Kansas City, KS, 66160, USA.
Bruce F KimlerDepartment of Radiation Oncology, Kansas University Medical Center, Kansas City, KS, 66160, USA.
Warren B NothnickDepartment of Molecular and Integrative Physiology, Kansas University Medical Center, Kansas City, KS, 66160, USA.
Marilyn K DavisDepartment of Pathology and Laboratory Medicine, Kansas University Medical Center, Kansas City, KS, 66160, USA.
Fang FanDepartment of Pathology and Laboratory Medicine, Kansas University Medical Center, Kansas City, KS, 66160, USA.
Ossama TawfikDepartment of Pathology and Laboratory Medicine, Kansas University Medical Center, Kansas City, KS, 66160, USA. Electronic address: otawfik@kumc.edu.
University Medical Center · USUniversity of Kansas Medical Center · US

Funding

The Role of miR-451 in Endometriosis Pathophysiology and TreatmentR01HD069043 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI NOTHNICK, WARREN B · 2012 to 2016
$1.7M
NICHD NIH HHS R01 HD069043NICHD NIH HHS R01HD0690431-01A1
6 · The paper itself

Abstract

Triple negative (TN) (estrogen receptor [ER], progesterone receptor [PR] and HER2-) are highly aggressive, rapidly growing, hormone-unresponsive tumors diagnosed at later stage that affect younger women with shorter overall survival. Most TN tumors are of the basal type. For the remainder, identification of target markers for effective treatment strategies remains a challenge. Transgelin (TGLN) is a 22-kd actin-binding protein of the calponin family. It is one of the earliest markers of smooth muscle differentiation. TGLN has been shown to have important biologic activities including regulating muscle fiber contractility, cell migration, and tumor suppression. We examined TGLN expression in the different molecular subtypes of breast cancer. TGLN expression was examined as a function of tumor size, grade, histologic type, lymph node status, patients' age and overall survival, ER, PR, HER2, and Ki-67 in 101 tumors that included 35 luminal A, 28 luminal B, 4 HER2, and 34 TN types. TGLN positivity (defined as 2+ or 3+) was associated with more aggressive tumors (10% of grade I/II tumors were TGLN+ versus 53% of grade III tumors; P < .001), high Ki-67 count, and low ER and PR expression (P < .001) but not with tumor size, age, or lymph node metastasis. TN (n = 34) tumors were 7.7 times more likely to be TGLN+ than non-TN (n = 67) tumors (77% versus 10%, respectively; P < .001). TGLN may be an excellent diagnostic marker of TN tumors and could be useful in stratification of patients. TGLN may also prove a potential target for future treatment strategies.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesFemaleHumansKi-67 AntigenMicrofilament ProteinsMiddle AgedMuscle ProteinsPrognosisReceptors, EstrogenReceptors, ProgesteroneTriple Negative Breast NeoplasmsBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesKi-67 AntigenMicrofilament ProteinsMuscle ProteinsReceptors, EstrogenReceptors, ProgesteronetransgelinInvasive breast cancerMolecular subtypesPrognostic markersTransgelinTriple-negative

Identifiers

PMID25841305
PMCPMC4426210
OpenAlexW2070009765

What OpenQuestion holds

Textmetadata
LicenceTDM
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.