Evidence map›Paper›PMID 38638038›Full record

ArticleCurrent medicinal chemistry2025

Astaxanthin as an Anticancer Agent against Breast Cancer: An

Maryam Shokrian Zeini, Seyyed Mohammad Pakravesh, Seyed Mostafa Jalili Kolour, Shahrad Soghala, Mohammad Amin Dabbagh Ohadi, Haniyeh Ghanbar Ali Akhavan, Zeinab Sayyahi, Lena Mahya, Saleheh Jahani, Sadegh Shojaei Baghini and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Current medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. 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

13 authors at 10 institutions in 3 countries.

Maryam Shokrian ZeiniDepartment of Biomedical Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND, United States.
Seyyed Mohammad PakraveshDepartment of Biotechnology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Seyed Mostafa Jalili KolourCellular and Molecular Biology master student, Department of Life Sciences and Systems Biology, University of Turin, Italy.
Shahrad SoghalaDepartment of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Mohammad Amin Dabbagh OhadiStudents'Scientific Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Haniyeh Ghanbar Ali AkhavanSchool of Medicine, Arak University of Medical Sciences, Arak, Iran.
Zeinab SayyahiDepartment of Physiology, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Lena MahyaCoenzyme R Research Institute, Tehran, Iran.
Saleheh JahaniCoenzyme R Research Institute, Tehran, Iran.
Sadegh Shojaei BaghiniPlant Biotechnology Department, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran.
Tahereh FarkhondehDepartment of Toxicology and Pharmacology, School of Pharmacy, Birjand University of Medical Sciences, Birjand, Iran.
Mahboubeh KabiriDepartment of Biotechnology, College of Science, University of Tehran, Tehran, Iran.
Saeed SamarghandianHealthy Ageing Research Centre, Neyshabur University of Medical Sciences, Neyshabur, Iran.
Islamic Azad University, Science and Research Branch · IRArak University of Medical Sciences · IRBirjand University of Medical Sciences · IRHamedan University of Medical Sciences · IRNational Institute of Genetic Engineering and Biotechnology · IRTehran University of Medical Sciences · IRUniversity of Neyshabur · IRUniversity of North Dakota · USUniversity of Tehran · IRUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThis study aimed to investigate the antioxidant properties, cytotoxic activity, and apoptotic effects of astaxanthin (ASX) on genes and pathways involved in breast cancer in Balb/c mice models injected with the 4T1 cell line.

backgroundASX could inhibit some tumor progression by using

objectiveThe effect of ASX on breast cancer was not fully understood till now.

methodIn an

resultsASX (200 mg/kg) caused a significant reduction in the mitotic cell count of tumor tissues compared to ASX (100 mg/kg). The antiproliferative effects of different concentrations of ASX were shown based on the MTT results. The treatment of breast tumor mice with both concentrations of ASX, especially 200 mg/kg, elevated the expression of

conclusionASX can be considered a promising alternative treatment for breast cancer.

Indexed as

Antineoplastic AgentsBreast NeoplasmsAnimalsApoptosisCell Line, TumorCell ProliferationDose-Response Relationship, DrugDrug Screening Assays, AntitumorFemaleHumansMiceMice, Inbred BALB CXanthophyllsAntineoplastic AgentsastaxanthineXanthophyllsapoptosisAstaxanthinbreast cancercytotoxicityMDA enzyme.oxidative stressSOD enzyme

Identifiers

PMID38638038
OpenAlexW4394958618

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.