Evidence map›Paper›PMID 26519257›Full record

ArticleMedical oncology (Northwood, London, England)2015

The role of interleukin-8 (CXCL8) and CXCR2 in acquired chemoresistance of human colorectal carcinoma cells HCT116.

Daiva Dabkeviciene, Violeta Jonusiene, Vilmante Zitkute, Egle Zalyte, Pranas Grigaitis, Vida Kirveliene, Ausra Sasnauskiene

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 12% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Anticancer Properties of Garlic and Ginger Extract in Colon Cancer Cell Line.Asian Pacific journal of cancer prevention : APJCP · 2024
    Article
  13. Review
  14. Review
  15. Therapeutic inhibition of CXCR1/2: where do we stand?Internal and emergency medicine · 2023
    Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. 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

7 authors at 1 institution in 1 country.

Daiva DabkevicieneDepartment of Biochemistry and Molecular Biology, Faculty of Natural Sciences, Vilnius University, Vilnius, Lithuania. daiva.dabkeviciene@gf.vu.lt.ORCID http://orcid.org/0000-0003-3261-7622
Violeta JonusieneDepartment of Biochemistry and Molecular Biology, Faculty of Natural Sciences, Vilnius University, Vilnius, Lithuania.
Vilmante ZitkuteDepartment of Biochemistry and Molecular Biology, Faculty of Natural Sciences, Vilnius University, Vilnius, Lithuania.
Egle ZalyteDepartment of Biochemistry and Molecular Biology, Faculty of Natural Sciences, Vilnius University, Vilnius, Lithuania.
Pranas GrigaitisDepartment of Biochemistry and Molecular Biology, Faculty of Natural Sciences, Vilnius University, Vilnius, Lithuania.
Vida KirvelieneDepartment of Biochemistry and Molecular Biology, Faculty of Natural Sciences, Vilnius University, Vilnius, Lithuania.
Ausra SasnauskieneDepartment of Biochemistry and Molecular Biology, Faculty of Natural Sciences, Vilnius University, Vilnius, Lithuania.
Vilnius University · LT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer is one of the most common malignant diseases and is a leading cause of cancer mortality in the Western world. Primary or acquired resistance to chemotherapeutic drugs is a common phenomenon which causes a failure in cancer treatment. A diverse range of molecular mechanisms has been implicated in drug resistance: DNA damage repair, alterations in drug metabolism, mutation of drug targets, increased rates of drug efflux, and activation of survival signaling pathways. The aim of this study was to investigate the expression of CXCL8-CXCR1/2 pathway, its impact on cell proliferation and cytokine expression in human colorectal carcinoma HCT116 cells, and their chemotherapy-resistant subline. We found that IL-1 alpha stimulates the production of CXCL8 through IL-1 receptor signaling. Our data indicate that CXCL8 is upregulated in chemoresistant subline of colorectal cancer cells HCT116, and modulation of CXCR2 pathway can be a target for proliferation inhibition of chemoresistant colorectal cancer cells.

Indexed as

Antineoplastic AgentsCell ProliferationCell SurvivalDrug Resistance, NeoplasmFluorouracilHCT116 CellsHumansInterleukin-1alphaInterleukin-8Organoplatinum CompoundsOxaliplatinReal-Time Polymerase Chain ReactionReceptors, Interleukin-8BSignal TransductionAntineoplastic AgentsCXCL8 protein, humanFluorouracilInterleukin-1alphaInterleukin-8Organoplatinum CompoundsOxaliplatinReceptors, Interleukin-8B5-fluorouracilChemoresistanceCXCL8CXCR2Interleukin-1 alphaOxaliplatin

Identifiers

PMID26519257
OpenAlexW2270343381

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.