Evidence map›Paper›PMID 15024062›Full record

ArticleMolecular and cellular biology2004

Securin is a target of the UV response pathway in mammalian cells.

Francisco Romero, Ana M Gil-Bernabé, Carmen Sáez, Miguel A Japón, José A Pintor-Toro, María Tortolero

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 45 citations in OpenAlex.

  1. SCF(FBXW7)-mediated degradation of p53 promotes cell recovery after UV-induced DNA damage.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
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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

6 authors at 3 institutions in 1 country.

Francisco RomeroDepartamento de Microbiología, Facultad de Biología, Universidad de Sevilla, 41013 Seville Spain. frport@us.es
Ana M Gil-Bernabé
Carmen Sáez
Miguel A Japón
José A Pintor-Toro
María Tortolero
Universidad de Sevilla · ESHospital Universitario Virgen del Rocío · ESInstituto de Recursos Naturales y Agrobiología de Sevilla · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

All eukaryotic cells possess elaborate mechanisms to protect genome integrity and ensure survival after DNA damage, ceasing proliferation and granting time for DNA repair. Securin is an inhibitory protein that is bound to a protease called Separase to inhibit sister chromatid separation until the onset of anaphase. At the metaphase-to-anaphase transition, Securin is degraded by the anaphase-promoting complex or cyclosome, and Separase contributes to the release of cohesins from the chromosome, allowing for the segregation of sister chromatids to opposite spindle poles. Here we provide evidence that human Securin (hSecurin) has a novel role in cell cycle arrest after exposure to UV light or ionizing radiation. In fact, irradiation downregulated the level of hSecurin protein, accelerating its degradation via the proteasome and reducing hSecurin mRNA translation, but the presence of hSecurin is necessary for cell proliferation arrest following UV treatment. Moreover, an alteration of UV-induced hSecurin downregulation could lead directly to the accumulation of DNA damage and the subsequent development of malignant tumors.

Indexed as

AnimalsApoptosisCaffeineCell CycleCell Cycle ProteinsCell DivisionCell LineCell SeparationCysteine EndopeptidasesDNA DamageEndopeptidasesFlow CytometryHumansMultienzyme ComplexesNeoplasm ProteinsProteasome Endopeptidase ComplexCaffeineCell Cycle ProteinsCysteine EndopeptidasesEndopeptidasesESPL1 protein, humanMultienzyme ComplexesNeoplasm Proteinspituitary tumor-transforming protein 1, humanProteasome Endopeptidase ComplexSecurinSeparaseTrans-Activators

Identifiers

PMID15024062
PMCPMC371137
OpenAlexW2171351760

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.