Evidence map›Paper›PMID 30744593›Full record

ArticleBMC cancer2019

Trefoil factors peptide-3 is associated with residual invasive breast carcinoma following neoadjuvant chemotherapy.

Suhail Al-Salam, Manjusha Sudhadevi, Aktham Awwad, Mohamed Al Bashir

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. TFF3 as a Diagnostic Biomarker in Kidney Transplant Patients.International journal of molecular sciences · 2023
    Article
  6. Article
  7. Article
  8. Article
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  10. Extracellular production of recombinantExperimental and therapeutic medicine · 2020
    Article
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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

4 authors at 2 institutions in 1 country.

Suhail Al-SalamDepartment of Pathology, College of Medicine & Health Sciences, United Arab Emirates University, AlAin, PO Box 17666, United Arab Emirates. suhaila@uaeu.ac.ae.
Manjusha SudhadeviDepartment of Pathology, College of Medicine & Health Sciences, United Arab Emirates University, AlAin, PO Box 17666, United Arab Emirates.
Aktham AwwadDepartment of Laboratory Medicine, Tawam Hospital, AlAin, United Arab Emirates.
Mohamed Al BashirDepartment of Surgery, Tawam Hospital, AlAin, United Arab Emirates.
Tawam Hospital · AEUnited Arab Emirates University · AE

Funding

College of Medicine and Health Sciences, United Arab Emirates University (AE) Grant NP-14-23
6 · The paper itself

Abstract

backgroundBreast carcinoma is the commonest cancer among UAE population and the most common cancer among females. Examination of the 5' promoter regions of trefoil factor 3 (TFF3) gene has identified putative estrogen and progesterone receptor-DNA binding domains as direct response elements to estrogen and progesterone that are linked to breast functions or steroid regulation. The study was designed to determine the role of TFF3 in breast cancer chemoresistance with the aim of establishing TFF3 expression as a biomarker for drug resistance.

methodsIn total, 133 cases of breast carcinoma treated with neo-adjuvant therapy were collected. Tissue samples from pre-neoadjuvant therapy as well as tissues from post-neo-adjuvant therapy of those cases were collected and stained with immunohistochemistry for TFF3, Bcl2, BAX, cleaved caspase-3, AKT-1, NF kappa B and Ki-67.

resultsThere was increased expression of TFF3 in residual invasive carcinoma cells. There was a significant correlation between the expression of TFF3 in breast carcinoma cells and response to neoadjuvant chemotherapy (p = 0.0165). There was significant co-expression of TFF3 with AKT1 (p = 0.0365), BCl2 (p = 0.0152), and NF Kappa-B (p = 0.0243) in breast carcinoma cases with residual carcinoma following neoadjuvant therapy which support the role of TFF3 in chemoresistance.

conclusionThe expression of TFF3 is significantly associated with residual breast carcinoma following neoadjuvant chemotherapy suggesting its expression is associated with increased resistance to chemotherapy. This is supported by its co-expression with antiapoptotic proteins; BCl2, AKT1 and NF Kappa-B in residual breast carcinoma cells and very low proliferating index and apoptotic bodies in residual tumors.

Indexed as

Biomarkers, TumorAdultAge FactorsApoptosisBiopsyBreast NeoplasmsCarcinoma, Ductal, BreastCell ProliferationChemotherapy, AdjuvantFemaleGene ExpressionHumansImmunohistochemistryMiddle AgedNeoadjuvant TherapyNeoplasm InvasivenessBiomarkers, TumorTFF3 protein, humanTrefoil Factor-3Breast carcinomaChemoresistanceTrefoil factor-3

Identifiers

PMID30744593
PMCPMC6371459
OpenAlexW2922344721

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.