Evidence map›Paper›PMID 26595411›Full record

ReviewNutrition and cancer2016

Cancer chemoprevention research with selenium in the post-SELECT era: Promises and challenges.

Junxuan Lü, Jinhui Zhang, Cheng Jiang, Yibin Deng, Nur Özten, Maarten C Bosland

Open access · greenAbstract readReview
In one paragraph

Review in Nutrition and cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
6.3field-weighted citation impact, top 3% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

  1. Selenium for preventing cancer.The Cochrane database of systematic reviews · 2018
    Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. The selenium paradox friend or foe in breast cancer?Annals of medicine and surgery (2012) · 2025
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Fractionation of selenium isotopes during biofortification of Saccharomyces cerevisiae and the influence of metabolic labeling withJournal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2023
    Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Observational
  17. Article
  18. Article
  19. Article
  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 2 countries.

Junxuan Lüa Department of Biomedical Sciences , School of Pharmacy, Texas Tech University Health Sciences Center , Amarillo , Texas , USA.
Jinhui Zhanga Department of Biomedical Sciences , School of Pharmacy, Texas Tech University Health Sciences Center , Amarillo , Texas , USA.
Cheng Jianga Department of Biomedical Sciences , School of Pharmacy, Texas Tech University Health Sciences Center , Amarillo , Texas , USA.
Yibin Dengb Hormel Institute, University of Minnesota , Austin , Minnesota , USA.
Nur Öztenc Department of Pathology , University of Illinois at Chicago, College of Medicine, Chicago, Illinois, USA and Department of Pharmaceutical Toxicology, Faculty of Pharmacy, Bezmiâlem Vakif University , Istanbul , Turkey.
Maarten C Boslandc Department of Pathology , University of Illinois at Chicago, College of Medicine, Chicago, Illinois, USA and Department of Pharmaceutical Toxicology, Faculty of Pharmacy, Bezmiâlem Vakif University , Istanbul , Turkey.
Texas Tech University Health Sciences Center · USUniversity of Illinois Chicago · USTexas Tech University · USUniversity of Minnesota · US

Funding

PREVENTION OF PROSTATE CARCINOGENESIS BY NEXT-GENERATION SELENIUMR01CA172169 · NCI · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI LU, JUNXUAN · 2013 to 2018
$1.6M
NCI NIH HHS R01 CA172169
6 · The paper itself

Abstract

The negative efficacy outcomes of double-blinded, randomized, placebo-controlled Phase III human clinical trials with selenomethionine (SeMet) and SeMet-rich selenized-yeast (Se-yeast) for prostate cancer prevention and Se-yeast for prevention of nonsmall cell lung cancer (NSCLC) in North America lead to rejection of SeMet/Se-yeast for cancer prevention in Se-adequate populations. We identify 2 major lessons from the outcomes of these trials: 1) the antioxidant hypothesis was tested in wrong subjects or patient populations, and 2) the selection of Se agents was not supported by cell culture and preclinical animal efficacy data as is common in drug development. We propose that next-generation forms of Se (next-gen Se), such as methylselenol precursors, offer biologically appropriate approaches for cancer chemoprevention but these are faced with formidable challenges. Solid mechanism-based preclinical efficacy assessments and comprehensive safety studies with next-gen Se will be essential to revitalize the idea of cancer chemoprevention with Se in the post-SELECT era. We advocate smaller mechanism-driven Phase I/II trials with these next-gen Se to guide and justify future decisions for definitive Phase III chemoprevention efficacy trials.

Indexed as

AnimalsAnticarcinogenic AgentsAntioxidantsChemopreventionClinical Trials as TopicHumansNeoplasmsProteomicsSelenium CompoundsThioredoxin-Disulfide ReductaseVitamin EAnticarcinogenic AgentsAntioxidantsSelenium CompoundsThioredoxin-Disulfide ReductaseVitamin E

Identifiers

PMID26595411
PMCPMC4822195
OpenAlexW2179295938

What OpenQuestion holds

Textmetadata
LicenceTDM
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.