Evidence map›Paper›PMID 27698925›Full record

ArticleJournal of Cancer2016

Low Proteolytic Clipping of Histone H3 in Cervical Cancer.

Jorge Sandoval-Basilio, Nicolás Serafín-Higuera, Octavio D Reyes-Hernandez, Idanya Serafín-Higuera, Gabriela Leija-Montoya, Magali Blanco-Morales, Monica Sierra-Martínez, Roberto Ramos-Mondragon, Silvia García, Luz Berenice López-Hernández and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Specific tracking of N-terminal clipping on histone H3 inMarine life science & technology · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. 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

12 authors at 2 institutions in 1 country.

Jorge Sandoval-BasilioÁrea de investigación clínica, Unidad de Innovación Clínica y Epidemiológica de la Secretaría de Salud del estado de Guerrero, Acapulco, Gro., México.; Laboratorio de Biología Molecular, Universidad Hipócrates, Acapulco, Gro., México.
Nicolás Serafín-HigueraLaboratorio de Biología Celular, Unidad Ciencias de la Salud, Facultad de Odontología, Universidad Autónoma de Baja California Mexicali, BC, México.
Octavio D Reyes-HernandezLaboratorio de Genética y Diagnóstico Molecular, Unidad de Investigación, Hospital Juárez de México, Ciudad de México, México.; Facultad de Estudios Superiores Zaragoza, Universidad Nacional Autónoma de México, Ciudad de México, México.
Idanya Serafín-HigueraUnidad Académica de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo, Gro., México.
Gabriela Leija-MontoyaLaboratorio de Bioquímica, Unidad Ciencias de la Salud, Facultad de Medicina Mexicali, Universidad Autónoma de Baja California Mexicali, BC, México.
Magali Blanco-MoralesÁrea de investigación clínica, Unidad de Innovación Clínica y Epidemiológica de la Secretaría de Salud del estado de Guerrero, Acapulco, Gro., México.
Monica Sierra-MartínezLaboratorio de Genética y Diagnóstico Molecular, Unidad de Investigación, Hospital Juárez de México, Ciudad de México, México.
Roberto Ramos-MondragonDepartment of internal Medicine, Center for Arrhythmia Research, University of Michigan.
Silvia GarcíaCentro Médico Nacional 20 de Noviembre, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Ciudad de México, México.
Luz Berenice López-HernándezCentro Médico Nacional 20 de Noviembre, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Ciudad de México, México.
Martha Yocupicio-MonroyPosgrado en Ciencias Genómicas, Universidad Autónoma de la Ciudad de México, Ciudad de México, México.
Sofia L Alcaraz-EstradaCentro Médico Nacional 20 de Noviembre, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Ciudad de México, México.
Institute for Social Security and Services for State Workers · MXUniversidad Autónoma de la Ciudad de México · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chromatin in cervical cancer (CC) undergoes chemical and structural changes that alter the expression pattern of genes. Recently, a potential mechanism, which regulates gene expression at transcriptional levels is the proteolytic clipping of histone H3. However, until now this process in CC has not been reported. Using HeLa cells as a model of CC and human samples from patients with CC, we identify that the H3 cleavage was lower in CC compared with control tissue. Additionally, the histone H3 clipping was performed by serine and aspartyl proteases in HeLa cells. These results suggest that histone H3 clipping operates as part of post-translational modification system in CC.

Indexed as

Cervical cancerHeLa.Histone 3Histone H3 clippingHistone modificationsHistone proteolysis

Identifiers

PMID27698925
PMCPMC5039369
OpenAlexW2520935393

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.