Evidence map›Paper›PMID 38165473›Full record

ReviewMedical oncology (Northwood, London, England)2024

COX 2-inhibitors; a thorough and updated survey into combinational therapies in cancers.

Paul Rodrigues, Harun Bangali, Ahmad Hammoud, Yasser Fakri Mustafa, Hussein Riyadh Abdul Kareem Al-Hetty, Adnan Taan Alkhafaji, Maha Medha Deorari, Muataz Mohammed Al-Taee, Rahman S Zabibah, Ali Alsalamy

Abstract readReview
PubMed Publisher
In one paragraph

Review in Medical oncology (Northwood, London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
18.4field-weighted citation impact, top 1% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
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  3. Complete response in disseminatedTranslational lung cancer research · 2026
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  5. Analysis of Two New Flavonoid Glycosides FromAnalytical science advances · 2026
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  7. Cell-Free DNA-Based Theranostics for Inflammatory Disorders.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  8. Insights into Bioactive Constituents from Pericarp ofAntioxidants (Basel, Switzerland) · 2026
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  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

10 authors at 9 institutions in 5 countries.

Paul RodriguesDepartment of Computer Engineering, College of Computer Science, King Khalid University, Al-Faraa, Asir-Abha, Kingdom of Saudi Arabia.
Harun BangaliDepartment of Computer Engineering, College of Computer Science, King Khalid University, Al-Faraa, Asir-Abha, Kingdom of Saudi Arabia.
Ahmad HammoudDepartment of Medical and Technical Information Technology, Bauman Moscow State Technical University, Moscow, Russia. hammoud.a@mail.ru.ORCID http://orcid.org/0009-0001-7581-9024
Yasser Fakri MustafaDepartment of Pharmaceutical Chemistry, College of Pharmacy, University of Mosul, Mosul, 41001, Iraq.
Hussein Riyadh Abdul Kareem Al-HettyDepartment of Biology, College of Education For Pure Sciences, University of Anbar, Ramadi, Anbar, Iraq. hussin.riyadh@uoanbar.edu.iq.
Adnan Taan AlkhafajiCardiology Department, College of Medicine, Al-Ayen University, Thi-Qar, Iraq.
Maha Medha DeorariUttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, India.
Muataz Mohammed Al-TaeeDepartment of Medical Laboratories Technology, AL-Nisour University College, Baghdad, Iraq.
Rahman S ZabibahCollege of Medical Technique, the Islamic University, Najaf, Iraq.
Ali AlsalamyCollege of Technical Engineering, Imam Ja'afar Al-Sadiq University, Al-Muthanna, 66002, Iraq.
King Khalid University · SAAl-Nisour University College · IQBauman Moscow State Technical University · RUImam Ja’afar Al-Sadiq UniversityIraqi University · IQThi Qar University · IQUniversity of Anbar · IQUniversity of Mosul · IQUttaranchal University · IN

Funding

Deanship of Scientific Research, King Khalid University RGP2/420/44
6 · The paper itself

Abstract

Cyclooxygenase (COX) enzymes are pivotal in inflammation and cancer development. COX-2, in particular, has been implicated in tumor growth, angiogenesis, and immune evasion. Recently, COX-2 inhibitors have arisen as potential therapeutic agents in cancer treatment. In addition, combining COX inhibitors with other treatment modalities has demonstrated the potential to improve therapeutic efficacy. This review aims to investigate the effects of COX inhibition, both alone and in combination with other methods, on signaling pathways and carcinogenesis in various cancers. In this study, a literature search of all major academic databases was conducted (PubMed, Scholar google), including the leading research on the mechanisms of COX-2, COX-2 inhibitors, monotherapy with COX-2 inhibitors, and combining COX-2-inhibitors with chemotherapeutic agents in tumors. The study encompasses preclinical and clinical evidence, highlighting the positive findings and the potential implications for clinical practice. According to preclinical studies, multiple signaling pathways implicated in tumor cell proliferation, survival, invasion, and metastasis can be suppressed by inhibiting COX. In addition, combining COX inhibitors with chemotherapy drugs, targeted therapies, immunotherapies, and miRNA-based approaches has enhanced anti-tumor activity. These results suggest that combination therapy has the potential to overcome resistance mechanisms and improve treatment outcomes. However, caution must be exercised when selecting and administering combination regimens. Not all combinations of COX-2 inhibitors with other drugs result in synergistic effects; some may even have unfavorable interactions. Therefore, personalized approaches that consider the specific characteristics of the cancer and the medications involved are crucial for optimizing therapeutic strategies. In conclusion, as monotherapy or combined with other methods, COX inhibition bears promise in modulating signaling pathways and inhibiting carcinogenesis in various cancers. Additional studies and well-designed clinical trials are required to completely elucidate the efficacy of COX inhibition and combination therapy in enhancing cancer treatment outcomes. This narrative review study provides a detailed summary of COX-2 monotherapy and combination targeted therapy in cancer treatment.

Indexed as

Cyclooxygenase 2 InhibitorsNeoplasmsCarcinogenesisCombined Modality TherapyCyclooxygenase 2HumansCyclooxygenase 2Cyclooxygenase 2 InhibitorsCancerCombinational therapyCOX-2COX-2 inhibitor

Identifiers

PMID38165473
OpenAlexW4390507466

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.