Evidence map›Paper›PMID 41089196›Full record

ReviewExperimental and therapeutic medicine2025

Potential of CXCR1/2 as a target for the treatment of inflammation and cancer (Review).

Jing-Ming Zhong, Jing-Wei He, Ying Xiong, Meng-Ze Li

Abstract readReview
In one paragraph

Review in Experimental and therapeutic medicine, 2025. 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
–field-weighted citation impact
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.

  1. Interleukin-8 in health and disease.Molecular biomedicine · 2026
    Review
  2. Review
  3. Article
  4. Article
  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

4 authors.

Jing-Ming ZhongDepartment of Pathology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Jing-Wei HeDepartment of Pathology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Ying XiongDepartment of Pathology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Meng-Ze LiDepartment of Orthopedics, Luzhou Traditional Chinese Medicine Hospital, Luzhou, Sichuan 646000, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

C-X-C motif chemokine receptor (CXCR)1 and CXCR2 are chemokine receptors that serve critical roles in mediating immune and inflammatory responses. Their activation by chemokines, such as C-X-C motif chemokine ligand (CXCL)8/IL-8, can promote cell migration, proliferation and the release of additional inflammatory mediators, contributing to the progression of inflammatory diseases and cancers. By inhibiting the binding of CXCL8/IL-8 to CXCR1 and CXCR2, SCH527123 aims to disrupt these harmful processes and offers a promising therapeutic strategy. Research on immunotherapy, particularly focusing on targeting specific immune receptors and pathways, is experiencing a surge of interest and progress. Exploration of SCH527123 as a novel CXCR1 and CXCR2 antagonist has highlighted the potential of this approach in treating various diseases, particularly those involving inflammation and cancers. The preclinical success of SCH527123 in animal models of liver, pancreatic and ovarian cancers has underscored its potential as an anti-inflammatory and anti-tumor agent. These findings suggest that targeting CXCR1/2 signaling may represent a viable approach for treating a broad range of malignancies. Furthermore, interest in SCH527123 as a potential treatment for COPD and asthma has suggested its potential applications beyond cancer therapy. Therefore, SCH527123 represents a new drug candidate with potential in the fields of inflammation and cancer. Although challenges remain in translating preclinical findings into clinical benefits, ongoing research and development efforts on using SCH527123 hold promise for improving the survival and quality of life of patients with these devastating diseases.

Indexed as

cancersC-X-C motif chemokine receptorIL-8inflammationSCH527123

Identifiers

PMID41089196
PMCPMC12516482

What OpenQuestion holds

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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.