Evidence map›Paper›PMID 27854258›Full record

ArticleMolecules (Basel, Switzerland)2016

Antiproliferative, Cytotoxic, and Apoptotic Activity of Steroidal Oximes in Cervicouterine Cell Lines.

Luis Sánchez-Sánchez, María Guadalupe Hernández-Linares, María L Escobar, Hugo López-Muñoz, Edgar Zenteno, María A Fernández-Herrera, Gabriel Guerrero-Luna, Alan Carrasco-Carballo, Jesús Sandoval-Ramírez

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 25 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Luis Sánchez-SánchezFacultad de Estudios Superiores Zaragoza, Universidad Nacional Autónoma de México, 09230 Ciudad de México, Mexico. luisss@unam.mx.
María Guadalupe Hernández-LinaresLaboratorio de Investigación, Jardín Botánico Universitario, Benemérita Universidad Autónoma de Puebla, 72570 Puebla, Pue., Mexico. guadalupe.mghl@correo.buap.mx.
María L EscobarDepartamento de Biología Celular, Facultad de Ciencias, Universidad Nacional Autónoma de México, 04510 Ciudad de México, Mexico. escobarluisa@ciencias.unam.mx.
Hugo López-MuñozFacultad de Estudios Superiores Zaragoza, Universidad Nacional Autónoma de México, 09230 Ciudad de México, Mexico. hugogris@hotmail.com.
Edgar ZentenoDepartamento de Bioquímica, Facultad de Medicina, Universidad Nacional Autónoma de México, 04510 Ciudad de México, Mexico. ezenteno@unam.mx.
María A Fernández-HerreraDepartamento de Física Aplicada, Centro de Investigación y de Estudios Avanzados-Unidad Mérida, km 6 Antigua Carretera a Progreso, Cordemex, 97310 Mérida, Yuc., Mexico. mfernandez@cinvestav.mx.
Gabriel Guerrero-LunaLaboratorio de Investigación, Jardín Botánico Universitario, Benemérita Universidad Autónoma de Puebla, 72570 Puebla, Pue., Mexico. gabriel.guerrero@alumno.buap.mx.
Alan Carrasco-CarballoLaboratorio de Investigación, Jardín Botánico Universitario, Benemérita Universidad Autónoma de Puebla, 72570 Puebla, Pue., Mexico. alan.carballo@alumno.buap.mx.
Jesús Sandoval-RamírezFacultad de Ciencias Químicas, Benemérita Universidad Autónoma de Puebla, 72570 Puebla, Pue., Mexico. jesus.sandoval@correo.buap.mx.
Benemérita Universidad Autónoma de Puebla · MXUniversidad Nacional Autónoma de México · MXUniversidad Marista de Mérida · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Steroidal sapogenins have shown antiproliferative effects against several tumor cell lines; and their effects on human cancer cells are currently under study. Changes in the functionality on the steroidal structure make it possible to modify the biological activity of compounds. Herein, we report the synthesis and in vitro antitumor activity of two steroidal oxime compounds on cervical cancer cells. These derivatives were synthesized from the steroidal sapogenin diosgenin in good yields. The in vitro assays show that the steroidal oximes show significant antiproliferative activity compared to the one observed for diosgenin. Cell proliferation, cell death, and the cytotoxic effects were determined in both cervical cancer cells and human lymphocytes. The cancer cells showed apoptotic morphology and an increased presence of active caspase-3, providing the notion of a death pathway in the cell. Significantly, the steroidal oximes did not exert a cytotoxic effect on lymphocytes.

Indexed as

Antineoplastic AgentsApoptosisCaspase 3Cell CycleCell Line, TumorCell ProliferationCell SurvivalDiosgeninDrug Screening Assays, AntitumorFemaleGene Expression Regulation, NeoplasticHeLa CellsHumansOximesSignal TransductionSteroidsAntineoplastic AgentsCASP3 protein, humanCaspase 3DiosgeninOximesSteroids23-acetyldiosgenin(25R)-spirost-4-en-3,6-dioneantiproliferative activityapoptosissteroidal oximes

Identifiers

PMID27854258
PMCPMC6273349
OpenAlexW2550362351

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.