Evidence map›Paper›PMID 31516560›Full record

ReviewOncology letters2019

Cervical cancer stem cells and other leading factors associated with cervical cancer development.

Gretel Mendoza-Almanza, Elizabeth Ortíz-Sánchez, Leticia Rocha-Zavaleta, César Rivas-Santiago, Edgar Esparza-Ibarra, Jorge Olmos

Open access · diamondAbstract readReview
In one paragraph

Review in Oncology letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  5. Article
  6. Review
  7. Review
  8. Review
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  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Cervical Carcinoma: Oncobiology and Biomarkers.International journal of molecular sciences · 2021
    Review
  17. Review
  18. Review
  19. Review
  20. 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

6 authors at 4 institutions in 1 country.

Gretel Mendoza-AlmanzaNational Council for Science and Technology, Autonomous University of Zacatecas, Zacatecas 98060, Mexico.
Elizabeth Ortíz-SánchezBasic Research Division, National Cancer Institute, Mexico City 14080, Mexico.
Leticia Rocha-ZavaletaInstitute of Biomedical Research, National Autonomous University of Mexico, Mexico City 04510, Mexico.
César Rivas-SantiagoNational Council for Science and Technology, Autonomous University of Zacatecas, Zacatecas 98060, Mexico.
Edgar Esparza-IbarraAcademic Unit of Biological Sciences, Autonomous University of Zacatecas, Zacatecas 98060, Mexico.
Jorge OlmosDepartment of Marine Biotechnology, Center for Scientific Research and Higher Education, Ensenada 22860, Mexico.
Universidad Autónoma de Zacatecas "Francisco García Salinas" · MXEnsenada Institute of Technology · MXInstituto Nacional de Cancerología · MXUniversidad Nacional Autónoma de México · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer (CC) is one of the leading causes of cancer-associated mortalities in women from developing countries. Similar to other types of cancer, CC is considered to be a multifactorial disease, involving socioeconomic, cultural, immunological and epigenetic factors, as well as persistent human papilloma virus (HPV) infection. It has been well established that cancer stem cells (CSCs) play an important role in defining tumor size, the speed of development and the level of regression following treatment; therefore, CSCs are associated with a poor prognosis. CSCs have been detected in many types of cancer, including leukemia, pancreatic, colon, esophagus, liver, prostate, breast, gastric and lung cancer. In cervical cancer, CSCs have been associated with resistance to normally used drugs such as cisplatin. The present review summarizes the strategies that high-risk HPV viruses (HPV-16 and HPV-18) have developed to transform normal epithelial cells into cancer cells, as well as the cellular pathways and studies associated with the identification of cervical cancer stem cell biomarkers. In this sense, the present review provides state of the art information regarding CC development.

Indexed as

biomarkers of cancer stem cellscervical cancercervical cancer stem cellshuman papillomavirus

Identifiers

PMID31516560
PMCPMC6733009
OpenAlexW2965371519

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.