Evidence map›Paper›PMID 36911097›Full record

ArticleCancer research communications2023

Tumor-derived GCSF Alters Tumor and Systemic Immune System Cell Subset Composition and Signaling.

Israel Matos, Maunish Barvalia, Manreet K Chehal, A Gordon Robertson, Iva Kulic, Jessica A F D Silva, Abhinandan Ranganathan, Amy Short, Yu-Hsuan Huang, Erin Long and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancer research communications, 2023. 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
0.7field-weighted citation impact, top 29% 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, 4 citations in OpenAlex.

  1. Article
  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

15 authors at 4 institutions in 1 country.

Israel MatosDepartment of Microbiology and Immunology, University of British Columbia, Life Sciences Institute, Vancouver, British Columbia, Canada.ORCID 0000-0002-7269-6137
Maunish BarvaliaDepartment of Microbiology and Immunology, University of British Columbia, Life Sciences Institute, Vancouver, British Columbia, Canada.ORCID 0000-0003-0226-6411
Manreet K ChehalDepartment of Microbiology and Immunology, University of British Columbia, Life Sciences Institute, Vancouver, British Columbia, Canada.ORCID 0000-0003-3497-4930
A Gordon RobertsonCanada's Michael Smith Genome Sciences Centre, BC Cancer Agency. Vancouver, British Columbia, Canada.ORCID 0000-0002-2839-596X
Iva KulicME Therapeutics Inc. Vancouver, British Columbia, Canada.ORCID 0000-0001-9093-113X
Jessica A F D SilvaDepartment of Microbiology and Immunology, University of British Columbia, Life Sciences Institute, Vancouver, British Columbia, Canada.ORCID 0000-0003-4637-5732
Abhinandan RanganathanDepartment of Microbiology and Immunology, University of British Columbia, Life Sciences Institute, Vancouver, British Columbia, Canada.ORCID 0000-0002-0641-1404
Amy ShortME Therapeutics Inc. Vancouver, British Columbia, Canada.ORCID 0000-0003-2674-6102
Yu-Hsuan HuangME Therapeutics Inc. Vancouver, British Columbia, Canada.ORCID 0000-0001-5711-5624
Erin LongME Therapeutics Inc. Vancouver, British Columbia, Canada.ORCID 0000-0002-2556-2689
John J PriatelME Therapeutics Inc. Vancouver, British Columbia, Canada.ORCID 0000-0001-8794-6306
Salim DhanjiME Therapeutics Inc. Vancouver, British Columbia, Canada.ORCID 0000-0001-7666-2690
Brad H NelsonDeeley Research Centre, BC Cancer, Victoria, British Columbia, Canada.ORCID 0000-0002-4445-5539
Danielle L KrebsDepartment of Microbiology and Immunology, University of British Columbia, Life Sciences Institute, Vancouver, British Columbia, Canada.ORCID 0000-0002-6522-7308
Kenneth W HarderDepartment of Microbiology and Immunology, University of British Columbia, Life Sciences Institute, Vancouver, British Columbia, Canada.ORCID 0000-0003-4847-1285
University of British Columbia · CAiCo Therapeutics (Canada) · CACanada's Michael Smith Genome Sciences Centre · CAUniversity of Victoria · CA

Funding

CIHR PJT-175326
6 · The paper itself

Abstract

While immunotherapies such as immune checkpoint blockade and adoptive T-cell therapy improve survival for a subset of human malignancies, many patients fail to respond. Phagocytes including dendritic cells (DC), monocytes, and macrophages (MF) orchestrate innate and adaptive immune responses against tumors. However, tumor-derived factors may limit immunotherapy effectiveness by altering phagocyte signal transduction, development, and activity. Using Cytometry by Time-of-Flight, we found that tumor-derived GCSF altered myeloid cell distribution both locally and systemically. We distinguished a large number of GCSF-induced immune cell subset and signal transduction pathway perturbations in tumor-bearing mice, including a prominent increase in immature neutrophil/myeloid-derived suppressor cell (Neut/MDSC) subsets and tumor-resident PD-L1 Significance: Tumor-derived GCSF leads to systemic immune population changes. GCSF blockade restores immune populations, improves immunotherapy, and reduces tumor size, paralleling human colorectal cancer data. GCSF inhibition may synergize with current immunotherapies to treat GCSF-secreting tumors.

Indexed as

Colonic NeoplasmsMyeloid-Derived Suppressor CellsAnimalsHumansLymphocytes, Tumor-InfiltratingMiceMyeloid CellsSignal Transduction

Identifiers

PMID36911097
PMCPMC9997410
OpenAlexW4320915582

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.