Evidence map›Paper›PMID 34128362›Full record

ArticleJournal of breast cancer2021

HOXD Antisense Growth-Associated Long Noncoding RNA Promotes Triple-Negative Breast Cancer Progression by Activating Wnt Signaling Pathway.

Chenguang Zhang, Ying Yang, Lina Yi, Xuelaiti Paizula, Wenting Xu, Xiuping Wu

Open access · goldAbstract read
In one paragraph

Article in Journal of breast cancer, 2021. 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
1.0field-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, 13 citations in OpenAlex.

  1. Review
  2. Mechanistic insights into HAGLROS-mediated therapy resistance in ovarian cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

6 authors at 3 institutions in 1 country.

Chenguang ZhangDepartment of Breast Surgery, The Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi, China.ORCID https://orcid.org/0000-0002-7102-163X
Ying YangEEG Room, Weifang Yidu Central Hospital, Weifang, China.ORCID https://orcid.org/0000-0002-8802-0385
Lina YiThe Second Ward of Breast Surgery, The Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi, China.ORCID https://orcid.org/0000-0002-2155-3371
Xuelaiti PaizulaThe Second Ward of Breast Surgery, The Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi, China.ORCID https://orcid.org/0000-0002-2153-9166
Wenting XuThe Second Ward of Breast Surgery, The Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi, China.ORCID https://orcid.org/0000-0002-4603-0964
Xiuping WuDepartment of Breast Surgery, Zhengxing Hospital, Zhangzhou, China. t0t995bknqb@163.com.ORCID https://orcid.org/0000-0002-8372-3305
Xinjiang Medical University · CN175th Hospital of People's Liberation Army · CNYidu Central Hospital of Weifang · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTriple-negative breast cancer (TNBC) is the most lethal subtype of breast cancer owing to high heterogeneity, aggressive nature, and lack of treatment options, which has a substantial deleterious effect on patients' lives. HOXD antisense growth-associated long noncoding RNA (lncRNA) (HAGLR) plays tumor-promoting roles in many cancers. In this study, we aimed to explore the role of HAGLR in TNBC.

methodsQuantitative real-time polymerase chain reaction assays were used to examine the expression of RNAs. Functional experiments were conducted to test the biological behavior of TNBC cells. Moreover, MS2-RNA immunoprecipitation, luciferase reporter, and RNA pull-down assays were conducted to verify the binding relationship between HAGLR, microRNA-143-5p (miR-143-5p), and serine- and arginine-rich splicing factor 1 (SRSF1).

resultsHAGLR was found to be highly expressed in TNBC tissues and cells, and inhibiting HAGLR suppressed cell proliferation, migration, and invasion and promoted cell apoptosis in TNBC. Meanwhile, miR-93-5p was shown to bind to HAGLR and SRSF1. In addition, SRSF1 plays an oncogenic role in TNBC. Importantly, HAGLR could activate the Wnt signaling pathway by sponging miR-93-5p to upregulate SRSF1; thus, accelerating TNBC progression.

conclusionHAGLR could promote the progression of TNBC through the miR-93-5p/SRSF1 axis to activate the Wnt signaling pathway.

Indexed as

MicroRNAsRNA, long noncodingTriple negative breast neoplasmsWnt signaling pathway

Identifiers

PMID34128362
PMCPMC8250102
OpenAlexW3160114667

What OpenQuestion holds

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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.