Evidence map›Paper›PMID 33615686›Full record

ArticleThe Kaohsiung journal of medical sciences2021

The depletion of Circ-PRKDC enhances autophagy and apoptosis in T-cell acute lymphoblastic leukemia via microRNA-653-5p/Reelin mediation of the PI3K/AKT/mTOR signaling pathway.

Zhang Ling, Zhi-Gang Fang, Jie-Yong Wu, Jia-Jun Liu

Open access · goldAbstract read
In one paragraph

Article in The Kaohsiung journal of medical sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Recent Progress of CircRNAs in Hematological Malignancies.International journal of medical sciences · 2024
    Review
  8. Article
  9. Review
  10. The roles and mechanisms of circular RNAs related to mTOR in cancers.Journal of clinical laboratory analysis · 2022
    Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
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 1 institution in 1 country.

Zhang LingDepartment of Hematology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Zhi-Gang FangDepartment of Hematology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Jie-Yong WuDepartment of Hematology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Jia-Jun LiuDepartment of Hematology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0001-7878-3680
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A range of circular (Circ) RNAs have been demonstrated to be of therapeutic significance for the treatment of acute lymphoblastic leukemia (ALL). Here, we investigated the mechanisms underlying the action of Circ-PRKDC and the microRNA-653-5p/Reelin (miR-653-5p/RELN) axis in T-cell ALL (T-ALL).Clinical specimens were obtained from patients with T-ALL (n = 39) and healthy controls (n = 30). In each specimen, we determined the expression levels of Circ-PRKDC, miR-653-5p, and RELN. Human T-ALL cells (Jurkat) were transfected with Circ-PRKDC- or miR-653-5p-related sequences to investigate cell proliferation, apoptosis, and autophagy. We also determined the levels of Circ-PRKDC, miR-653-5p, RELN, and signaling proteins related to phosphoinositide 3-kinase (PI3K), AKT, and mammalian target of rapamycin (mTOR). Finally, we decoded the interactions between Circ-PRKDC, miR-653-5p, and RELN. The expression levels of Circ-PRKDC and RELN were upregulated in T-ALL tissues and cells while the levels of miR-653-5p were downregulated. Thereafter, then silencing of Circ-PRKDC, or the enforced expression of miR-653-5p, repressed the expression of RELN and the activation of the PI3K/AKT/mTOR signaling pathway, thus enhancing cell autophagy and apoptosis, and disrupting cell proliferation. Circ-PRKDC acted a sponge for miR-653-5p while miR-653-5p targeted RELN. The knockdown of miR-653-5p abrogated the silencing of Circ-PRKDC-induced effects in T-ALL cells. The depletion of Circ-PRKDC elevated miR-653-5p to silence RELN-mediated PI3K/AKT/mTOR signaling activation, thereby enhancing autophagy and apoptosis in T-ALL cells.

Indexed as

AutophagyAdolescentAdultApoptosisCell Line, TumorCell ProliferationChildDNA-Activated Protein KinaseFemaleGene Expression ProfilingGene Expression Regulation, LeukemicHumansJurkat CellsMaleMicroRNAsPhosphatidylinositol 3-KinasesAKT1 protein, humanDNA-Activated Protein KinaseMicroRNAsMIRN653 microRNA, humanMTOR protein, humanPhosphatidylinositol 3-KinasesPRKDC protein, humanProto-Oncogene Proteins c-aktReelin ProteinRELN protein, humanRNA, CircularTOR Serine-Threonine Kinasescircular-PRKDCMicroRNA-653-5pPI3K/AKT/mTOR signalingReelinT-cell acute lymphoblastic leukemia

Identifiers

PMID33615686
PMCPMC11896430
OpenAlexW3132882192

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.