Evidence map›Paper›PMID 29795410›Full record

ReviewCancer gene therapy2018

MicroRNA21 and the various types of myeloid leukemia.

Mani Panagal, Senthil Kumar S R, Sivakurunathan P, Biruntha M, Karthigeyan M, Vincent Gopinathe, Pethanen Sivakumare, Durairaj Sekar

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cancer gene therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.4field-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

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. METTL3: a multifunctional regulator in diseases.Molecular and cellular biochemistry · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. miRNA-503 inhibition exerts anticancer effects and reduces tumor growth in mesothelioma.Journal of experimental & clinical cancer research : CR · 2025
    Article
  14. Review
  15. Article
  16. FAT1 Gene Expression in Iranian Acute Lymphoid and Myeloid Leukemia Patients.International journal of hematology-oncology and stem cell research · 2023
    Article
  17. Review
  18. Review
  19. Article
  20. Article
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

8 authors at 3 institutions in 1 country.

Mani PanagalDepartment of Biotechnology, Annai College of Arts and Science, Kumbakonam, Tamil Nadu, 612001, India.
Senthil Kumar S RSchool of Biological Science, St. Joseph's College, Tiruchirappalli, 620002, India.
Sivakurunathan PSchool of Bioscience, Department of Microbiology, Annamalai University, Chidambaram, Tamil Nadu, 608002, India.
Biruntha MDepartment of Animal Health and Management, Alagappa University, Karaikkudi, Tamil Nadu, 630003, India.
Karthigeyan MDepartment of Zoology, Arumugam Pillai Seethai Ammal College, Tiruppattur, Tamil Nadu, India.
Vincent GopinatheDepartment of Zoology, Arumugam Pillai Seethai Ammal College, Tiruppattur, Tamil Nadu, India.
Pethanen SivakumareDepartment of Zoology, Arumugam Pillai Seethai Ammal College, Tiruppattur, Tamil Nadu, India.
Durairaj SekarDepartment of Life Science, Kristu Jayanti College (Autonomous), Bangalore University, Bengaluru, 560064, India. duraimku@gmail.com.
Alagappa University · INAnnamalai University · INBangalore University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloid leukemia (ML) is heterogeneous cancer classified by abnormal growth of myeloid cells due to genetic aberrations and mutations. It is generally categorized by clonal disorders of hematopoietic stem cells and differentiation. The molecular mechanism behind the myeloid malignancies is not yet known, but recent sequencing analysis reveals all the mutated factors. As we know that there is currently no compromise on therapy for such types of malignancies and at the present painful process like chemotherapy and radiation therapy are not effective for the treatment of ML, so there is an urgent need to develop a non-invasive biomarker for different types of ML. MicroRNAs (MiRNAs) is a small non-coding RNAs that have been involved in a wide range of biological function and it is the main cause of the manifestation of many diseases. Among the reported MiRNAs, MIR-21 is considered to be an important MiRNA, which is frequently elevated in many types of types of cancer, suggesting that it plays an important role in cancer progressions. So far, there is no paper that signifies the role of miR-21 in all types of ML and the number of studies on the different category of ML is sparse. Therefore, the main thrust of this paper is to provide an overview of the current clinical evidence and significance of miR-21 in ML. It was found that MiR-21 was found to be normally upregulated in all types of ML, however, we summarize the important research findings surrounding the role of miR-21 in different types of ML.

Indexed as

Gene Expression Regulation, LeukemicUp-RegulationAnimalsHumansLeukemia, MyeloidMicroRNAsRNA, NeoplasmMicroRNAsMIRN21 microRNA, humanRNA, Neoplasm

Identifiers

PMID29795410
OpenAlexW2803657669

What OpenQuestion holds

Textmetadata
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.