Evidence map›Paper›PMID 18818206›Full record

ArticleThe Journal of biological chemistry2008

Down-regulation of micro-RNA-1 (miR-1) in lung cancer. Suppression of tumorigenic property of lung cancer cells and their sensitization to doxorubicin-induced apoptosis by miR-1.

Mohd W Nasser, Jharna Datta, Gerard Nuovo, Huban Kutay, Tasneem Motiwala, Sarmila Majumder, Bo Wang, Saul Suster, Samson T Jacob, Kalpana Ghoshal

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in The Journal of biological chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 181 papers.

0numbers the graph read from it
0cells of the map it votes in
181citing papers in PubMed
11.0field-weighted citation impact, top 2% 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

181 citing papers in PubMed, 358 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. The Risks of miRNA Therapeutics: In a Drug Target Perspective.Drug design, development and therapy · 2021
    Review
  8. Article
  9. Dual Effects of Non-Coding RNAs (ncRNAs) in Cancer Stem Cell Biology.International journal of molecular sciences · 2020
    Review
  10. Article
  11. Article
  12. Article
  13. MicroRNAs and Long Non-coding RNAs in c-Met-Regulated Cancers.Frontiers in cell and developmental biology · 2020
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. microRNA-1 Regulates NCC Migration and Differentiation by TargetingInternational journal of biological sciences · 2019
    Article
  20. Article

121 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Mohd W NasserDepartment of Molecular and Cellular Biochemistry and Pathology, Ohio State University, Columbus, Ohio 43210, USA.
Jharna Datta
Gerard Nuovo
Huban Kutay
Tasneem Motiwala
Sarmila Majumder
Bo Wang
Saul Suster
Samson T Jacob
Kalpana Ghoshal
The Ohio State University · US

Funding

PathologyP01CA101956 · NCI · OHIO STATE UNIVERSITY · PI BYRD, JOHN C. · 2006 to 2010
$11.4M
The Role of MicroRNA in HepatocarcinogenesisR21CA122694 · NCI · OHIO STATE UNIVERSITY · PI GHOSHAL, KALPANA · 2006 to 2007
$309k
NCI NIH HHS CA122695NCI NIH HHS P01 CA101956NCI NIH HHS P01CA101956NCI NIH HHS R21 CA122694
6 · The paper itself

Abstract

Micro-RNAs are approximately 21-25-nucleotide-long noncoding RNAs that regulate gene expression primarily at the post-transcriptional level in animals. Here, we report that micro-RNA-1 (miR-1), abundant in the cardiac and smooth muscles, is expressed in the lung and is down-regulated in human primary lung cancer tissues and cell lines. In situ hybridization demonstrated localization of miR-1 in bronchial epithelial cells. The tumor suppressor C/EBPalpha, frequently suppressed in lung cancer, reactivated miR-1 expression in the lung cancer cells. Repressed miR-1 was also activated in lung cancer cells upon treatment with a histone deacetylase inhibitor. These observations led us to examine the antitumorigenic potential of miR-1 in lung cancer cells. Expression of miR-1 in nonexpressing A549 and H1299 cells reversed their tumorigenic properties, such as growth, replication potential, motility/migration, clonogenic survival, and tumor formation in nude mice. Exogenous miR-1 significantly reduced expression of oncogenic targets, such as MET, a receptor tyrosine kinase, and Pim-1, a Ser/Thr kinase, frequently up-regulated in lung cancer. Similarly, the levels of two additional targets, FoxP1, a transcription factor with oncogeneic property, and HDAC4 that represses differentiation-promoting genes, were reduced in miR-1-expressing cells. Conversely, depletion of miR-1 facilitated N417 cell growth with concomitant elevation of these targets. Further, ectopic miR-1 induced apoptosis in A549 cells in response to the potent anticancer drug doxorubicin. Enhanced activation of caspases 3 and 7, cleavage of their substrate PARP-1, and depletion of anti-apoptotic Mcl-1 contributed to the sensitivity of miR-1-expressing cells to doxorubicin. Thus, miR-1 has potential therapeutic application against lung cancers.

Indexed as

AnimalsAntibiotics, AntineoplasticApoptosisCaspase 3Caspase 7Cell Line, TumorCell MovementCell SurvivalDown-RegulationDoxorubicinForkhead Transcription FactorsGene Expression Regulation, NeoplasticHistone DeacetylasesHumansLung NeoplasmsMiceAntibiotics, AntineoplasticCASP3 protein, humanCASP7 protein, humanCaspase 3Caspase 7DoxorubicinForkhead Transcription FactorsFOXP1 protein, humanHDAC4 protein, humanHistone DeacetylasesMcl1 protein, mouseMET protein, humanMicroRNAsMyeloid Cell Leukemia Sequence 1 ProteinPARP1 protein, humanPIM1 protein, humanPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-metProto-Oncogene Proteins c-pim-1Receptors, Growth FactorRepressor ProteinsRNA, Neoplasm

Identifiers

PMID18818206
PMCPMC2586284
OpenAlexW2042907812

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.