Evidence map›Paper›PMID 33808326›Full record

ArticleCells2021

Nuclear Translocation of SRPKs Is Associated with 5-FU and Cisplatin Sensitivity in HeLa and T24 Cells.

Ioanna Sigala, Maria Koutroumani, Anastasia Koukiali, Thomas Giannakouros, Eleni Nikolakaki

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. SRPKs: a promising therapeutic target in cancer.Clinical and experimental medicine · 2023
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. 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

5 authors at 2 institutions in 1 country.

Ioanna SigalaLaboratory of Biochemistry, Department of Chemistry, Aristotelian University, 54124 Thessaloniki, Greece.
Maria KoutroumaniCentre for Research and Technology-Hellas, Institute of Applied Biosciences, 57001 Thessaloniki, Greece.
Anastasia KoukialiLaboratory of Biochemistry, Department of Chemistry, Aristotelian University, 54124 Thessaloniki, Greece.
Thomas GiannakourosLaboratory of Biochemistry, Department of Chemistry, Aristotelian University, 54124 Thessaloniki, Greece.
Eleni NikolakakiLaboratory of Biochemistry, Department of Chemistry, Aristotelian University, 54124 Thessaloniki, Greece.
Aristotle University of Thessaloniki · GRCentre for Research and Technology Hellas · GR

Funding

EΔBM103 Program co-financed by the European Union (European Social Fund-ESF) and Greek national funds through the Operational Program "Human Resources Development, Education and Lifelong Learning 2014-2020". MIS 5047934
6 · The paper itself

Abstract

Serine/arginine protein kinases (SRPKs) phosphorylate Arg/Ser dipeptide-containing proteins that play crucial roles in a broad spectrum of basic cellular processes. The existence of a large internal spacer sequence that separates the bipartite kinase catalytic core and anchors the kinases in the cytoplasm is a unique structural feature of SRPKs. Here, we report that exposure of HeLa and T24 cells to DNA damage inducers triggers the nuclear translocation of SRPK1 and SRPK2. Furthermore, we show that nuclear SRPKs did not protect from, but on the contrary, mediated the cytotoxic effects of genotoxic agents, such as 5-fluorouracil (5-FU) and cisplatin. Confirming previous data showing that the kinase activity is essential for the entry of SRPKs into the nucleus, SRPIN340, a selective SRPK1/2 inhibitor, blocked the nuclear accumulation of the kinases, thus diminishing the cytotoxic effects of the drugs. ATR/ATM-dependent phosphorylation of threonine 326 and serine 408 in the spacer domain of SRPK1 was essential for the redistribution of the kinase to the nucleus. Substitution of either of these two residues to alanine or inhibition of ATR/ATM kinase activity abolished nuclear localization of SRPK1 and conferred tolerance to 5-FU treatment. These findings suggest that SRPKs may play an important role in linking cellular signaling to DNA damage in eukaryotic cells.

Indexed as

Ataxia Telangiectasia Mutated ProteinsCell DeathCell NucleusCisplatinCytoprotectionDNA DamageFluorouracilHeLa CellsHumansModels, BiologicalNiacinamidePhosphorylationPiperidinesProtective AgentsProtein Serine-Threonine KinasesProtein TransportAtaxia Telangiectasia Mutated ProteinsATR protein, humanCisplatinFluorouracilNiacinamidePiperidinesProtective AgentsProtein Serine-Threonine KinasesSRPIN340SRPK1 protein, human5-FUATMATRcisplatindrug resistancefixation for immunofluorescenceSRPK1SRPK2SR protein kinases

Identifiers

PMID33808326
PMCPMC8065462
OpenAlexW3151997409

What OpenQuestion 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 OpenQuestion graph.