Evidence map›Paper›PMID 35044463›Full record

ArticleJournal of cell science2022

PCTAIRE1 promotes mitotic progression and resistance against antimitotic and apoptotic signals.

Syed Qaaifah Gillani, Irfana Reshi, Nusrat Nabi, Misbah Un Nisa, Zarka Sarwar, Sameer Bhat, Thomas M Roberts, Jonathan M G Higgins, Shaida Andrabi

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 35% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Cyclin-dependent kinases: Masters of the eukaryotic universe.Wiley interdisciplinary reviews. RNA · 2023
    Review
  8. 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

9 authors at 3 institutions in 3 countries.

Syed Qaaifah GillaniDepartment of Biochemistry, University of Kashmir, Srinagar 190006, India.ORCID 0000-0003-0533-5611
Irfana ReshiDepartment of Biotechnology, University of Kashmir, Srinagar 190006, India.ORCID 0000-0001-7583-7073
Nusrat NabiDepartment of Biochemistry, University of Kashmir, Srinagar 190006, India.ORCID 0000-0001-7822-4731
Misbah Un NisaDepartment of Biochemistry, University of Kashmir, Srinagar 190006, India.ORCID 0000-0001-9006-9682
Zarka SarwarDepartment of Biochemistry, University of Kashmir, Srinagar 190006, India.ORCID 0000-0003-0247-6427
Sameer BhatDepartment of Biotechnology, University of Kashmir, Srinagar 190006, India.ORCID 0000-0003-1172-9297
Thomas M RobertsDana Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.ORCID 0000-0001-6453-3955
Jonathan M G HigginsBiosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.ORCID 0000-0001-6622-8268
Shaida AndrabiDepartment of Biochemistry, University of Kashmir, Srinagar 190006, India.ORCID 0000-0002-4114-4401
University of Kashmir · INHarvard University · USNewcastle University · GB

Funding

PROJECT 4: Interrogating PP2A Signaling in Human CancersP01CA203655 · NCI · DANA-FARBER CANCER INST · PI DECAPRIO, JAMES A. · 2017 to 2021
$8.0M
NCI NIH HHS P01 CA203655Wellcome Trust
6 · The paper itself

Abstract

PCTAIRE1 (also known as CDK16) is a serine-threonine kinase implicated in physiological processes like neuronal development, vesicle trafficking, spermatogenesis and cell proliferation. However, its exact role in cell division remains unclear. In this study, using a library screening approach, we identified PCTAIRE1 among several candidates that resisted mitotic arrest and mitotic cell death induced by polyomavirus small T (PolST) expression in mammalian cells. Our study showed that PCTAIRE1 is a mitotic kinase that localizes at centrosomes during G2 and at spindle poles as the cells enter mitosis, and then at the midbody during cytokinesis. We also report that PCTAIRE1 protein levels fluctuate through the cell cycle and reach their peak at mitosis, during which there is an increase in PCTAIRE1 phosphorylation as well. Interestingly, knockdown of PCTAIRE1 resulted in aberrant mitosis by interfering with spindle assembly and chromosome segregation. Further, we found that PCTAIRE1 promotes resistance of cancer cells to antimitotic drugs, and this underscores the significance of PCTAIRE1 as a potential drug target for overcoming chemotherapeutic resistance. Taken together, these studies establish PCTAIRE1 as a critical mediator of mitotic progression and highlight its role in chemotherapeutic resistance. This article has an associated First Person interview with the first author of the paper.

Indexed as

Antimitotic AgentsAnimalsCell Cycle ProteinsCentrosomeChromosome SegregationHeLa CellsHumansMaleMitosisPhosphorylationProtein Serine-Threonine KinasesSpindle ApparatusAntimitotic AgentsCell Cycle ProteinsProtein Serine-Threonine KinasesCDK16Chemotherapeutic resistanceMitotic arrestPCTAIRE1PLK1PP2A

Identifiers

PMID35044463
PMCPMC8918779
OpenAlexW4205652688

What Socratic 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 Socratic graph.