Evidence map›Paper›PMID 31083383›Full record

ReviewCancers2019

Gene Expression and miRNAs Profiling: Function and Regulation in Human Epidermal Growth Factor Receptor 2 (HER2)-Positive Breast Cancer.

Rasha M Sareyeldin, Ishita Gupta, Israa Al-Hashimi, Hamda A Al-Thawadi, Halema F Al Farsi, Semir Vranic, Ala-Eddin Al Moustafa

Abstract readReview
In one paragraph

Review in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact
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

37 citing papers in PubMed.

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  9. Methanolic Leaves Extract ofInternational journal of molecular sciences · 2025
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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

7 authors.

Rasha M SareyeldinCollege of Medicine, Qatar University, Doha 2713, Qatar. rasha.sareyeldin@gmail.com.
Ishita GuptaCollege of Medicine, Qatar University, Doha 2713, Qatar. ishugupta28@gmail.com.
Israa Al-HashimiCollege of Medicine, Qatar University, Doha 2713, Qatar. ia1507081@student.qu.edu.qa.
Hamda A Al-ThawadiCollege of Medicine, Qatar University, Doha 2713, Qatar. halthawadi@qu.edu.qa.
Halema F Al FarsiCollege of Medicine, Qatar University, Doha 2713, Qatar. halfarsi@qu.edu.qa.
Semir VranicCollege of Medicine, Qatar University, Doha 2713, Qatar. svranic@qu.edu.qa.ORCID 0000-0001-9743-7265
Ala-Eddin Al MoustafaCollege of Medicine, Qatar University, Doha 2713, Qatar. semir.vranic@gmail.com.ORCID 0000-0003-4452-3439

Funding

Qatar University QUCG-CMED-2018\2019-3Qatar University QUCP-CMED-2019-1Qatar University QUSD-CMED-2018-2Qatar University QUST-1-CMED-2019-18
6 · The paper itself

Abstract

Breast cancer is the second most common cause of cancer-related deaths among women worldwide. It is a heterogeneous disease with four major molecular subtypes. One of the subtypes, human epidermal growth factor receptor 2 (HER2)-enriched (HER2-positive) is characterized by the absence of estrogen and progesterone receptors and overexpression of HER2 receptor, and accounts for 15-20% of all breast cancers. Despite the anti-HER2 and cytotoxic chemotherapy, HER2 subtype is an aggressive disease with significant mortality. Recent advances in molecular biology techniques, including gene expression profiling, proteomics, and microRNA analysis, have been extensively used to explore the underlying mechanisms behind human breast carcinogenesis and metastasis including HER2-positive breast cancer, paving the way for developing new targeted therapies. This review focuses on recent advances on gene expression and miRNA status in HER2-positive breast cancer.

Indexed as

biomarkersbreast cancergene expression profilingHER2-positive breast cancermicroarraymiRNAs

Identifiers

PMID31083383
PMCPMC6562440

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.