Evidence map›Paper›PMID 32458655›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2020

LAT1 (SLC7A5) Overexpression in Negative Her2 Group of Breast Cancer: A Potential Therapy Target.

Khaldon Bodoor, Rowida Almomani, Mohammad Alqudah, Yazan Haddad, Walaa Samouri

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

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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

5 authors at 2 institutions in 2 countries.

Khaldon BodoorDepartment of Applied Biology, Jordan University of Science and Technology, Irbid, Jordan.
Rowida AlmomaniDepartment of Medical Laboratory Sciences, Jordan University of Science and Technology, Irbid, Jordan.
Mohammad AlqudahDepartment of Pathology, Jordan University of Science and Technology, Irbid, Jordan.ORCID 0000-0001-6877-1184
Yazan HaddadDepartment of Chemistry and Biochemistry, Mendel University in Brno, Zemedelska 1, Brno, Czech Republic.
Walaa SamouriDepartment of Pathology, Jordan University of Science and Technology, Irbid, Jordan.
Jordan University of Science and Technology · JOBrno University of Technology · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveHER2 negative carcinomas of the breast pose a challenge for treatment due to redundancies in potential drug targets and poor patient outcomes. Our aim was to investigate the role of L-type amino acid transporter - LAT1 as a potential prognosticator and a drug target.

methodsIn this retrospective work, we have studied the expression of LAT1 in 145 breast cancer tissues via immunohistochemistry. Overall survival analysis was used to evaluate patient outcome in various groups of our cohort.

resultsPositive LAT1 expression was found in 27 (84.4%) luminal A subtype, 27 (64.3%) luminal B/triple positive subtype, 29 (82.9%) triple negative subtype, and 24 (66.7%) HER2-only positive subtype (p=0.1). Interestingly, negative correlation was found between LAT1 and HER2; where positive expression of LAT1 was found in 56 (83.6%) cases in negative HER2 group and 51 (65.4%) cases from positive HER2 group (p=0.01). Unfortunately, we were unable to report significant survival differences when LAT1 expression was studied in the negative HER2 group. Nevertheless, five incidents of mortality (out of 55) were reported in LAT1+/HER2- group compared to none in the LAT1-/HER2- group (N=11).

conclusionOur findings of overexpression of LAT1 in negative HER2 group suggest a role of this protein as prognosticator and drug target in a challenging therapeutic cohort.<br />.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, Ductal, BreastCarcinoma, LobularErb-b2 Receptor Tyrosine KinasesFemaleFollow-Up StudiesGene Expression Regulation, NeoplasticHumansLarge Neutral Amino Acid-Transporter 1Lymphatic MetastasisMiddle AgedNeoplasm InvasivenessNeoplasm Recurrence, LocalBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesLarge Neutral Amino Acid-Transporter 1Receptors, EstrogenReceptors, ProgesteroneSLC7A5 protein, humanbreast cancerHER2LAT1SLC7A5

Identifiers

PMID32458655
PMCPMC7541863
OpenAlexW3029680933

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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.