Evidence map›Paper›PMID 38356054›Full record

ReviewThe Journal of membrane biology2024

Potential Role of Nrf2, HER2, and ALDH in Cancer Stem Cells: A Narrative Review.

Azadeh Fakhrioliaei, Sepideh Tanhaei, SeyedAbbas Pakmehr, Maha Noori Shakir, Maytham T Qasim, Maryam Hariri, Alireza Nouhi Kararoudi, Mohammad Valilo

Abstract readReview
PubMed Publisher
In one paragraph

Review in The Journal of membrane biology, 2024. 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
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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. The cross-talk between NRF2 and apoptosis in cancer.Medical molecular morphology · 2025
    Review
  5. Review
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

8 authors at 8 institutions in 3 countries.

Azadeh FakhrioliaeiFaculty of Pharmacy, Islamic Azad University, Tehran, Iran.
Sepideh TanhaeiKermanshah University of Medical Sciences, Kermanshah, Iran.
SeyedAbbas PakmehrSchool of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Maha Noori ShakirDepartment of Medical Laboratories Technology, AL-Nisour University College, Baghdad, Iraq.
Maytham T QasimDepartment of Anesthesia, College of Health and Medical Technology, Al-Ayen University, Thi-Qar, Iraq.
Maryam HaririDepartment of Pathobiology, Auburn University, Auburn, AL, 36832, USA.
Alireza Nouhi KararoudiDepartment of Biology, Faculty of Sciences, Rasht Branch, Islamic Azad University, Rasht, Iran.
Mohammad ValiloDpartment of Biochemistry, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran. valilo.biomed@gmail.com.
Al-Nisour University College · IQAuburn University · USIslamic Azad University Rasht Branch · IRIslamic Azad University, Tehran · IRKermanshah University of Medical Sciences · IRShiraz University of Medical Sciences · IRThi Qar University · IQUrmia University of Medical Sciences

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is one of the main causes of death among humans, second only to cardiovascular diseases. In recent years, numerous studies have been conducted on the pathophysiology of cancer, and it has been established that this disease is developed by a group of stem cells known as cancer stem cells (CSCs). Thus, cancer is considered a stem cell disease; however, there is no comprehensive consensus about the characteristics of these cells. Several different signaling pathways including Notch, Hedgehog, transforming growth factor-β (TGF-β), and WNT/β-catenin pathways cause the self-renewal of CSCs. CSCs change their metabolic pathways in order to access easy energy. Therefore, one of the key objectives of researchers in cancer treatment is to destroy CSCs. Nuclear factor erythroid 2-related factor 2 (Nrf2) plays an essential role in the protection of CSCs from reactive oxygen species (ROS) and chemotherapeutic agents by regulating antioxidants and detoxification enzymes. Human epidermal growth factor receptor 2 (HER2) is a member of the tyrosine kinase receptor family, which contributes to the protection of cancer cells against treatment and implicated in the invasion, epithelial-mesenchymal transition (EMT), and tumorigenesis. Aldehyde dehydrogenases (ALDHs) are highly active in CSCs and protect the cells against damage caused by active aldehydes through the regulation of aldehyde metabolism. On the other hand, ALDHs promote the formation and maintenance of tumor cells and lead to drug resistance in tumors through the activation of various signaling pathways, such as the ALDH1A1/HIF-1α/VEGF axis and Wnt/β-catenin, as well as changing the intracellular pH value. Given the growing body of information in this field, in the present narrative review, we attempted to shed light on the function of Nrf2, HER2, and ALDH in CSCs.

Indexed as

Aldehyde Dehydrogenasebeta CateninErb-b2 Receptor Tyrosine KinasesNeoplastic Stem CellsNF-E2-Related Factor 2AldehydesHumansNeoplasmsAldehyde DehydrogenaseAldehydesbeta CateninERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesNF-E2-Related Factor 2Aldehyde dehydrogenasesCancer stem cellsChemotherapyHER2Nuclear factor erythroid 2-related factor 2

Identifiers

PMID38356054
OpenAlexW4391807375

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.