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Abstract A017: Exploring the interplay between macrophage subtypes and colorectal cancer cell growth

2023· article· en· W4389227697 on OpenAlexaboutno aff
Chun-Te Chiang, Danielle Hixon, Nevart Mooradian, Pratiksha Kshetri, Scott Valena, Roy Lau, Charlie Ambrose, Michael E. Doche, Reginald Hill, Shannon M. Mumenthaler

Bibliographic record

VenueCancer Immunology Research · 2023
Typearticle
Languageen
FieldImmunology and Microbiology
TopicImmune cells in cancer
Canadian institutionsnot available
Fundersnot available
KeywordsTumor microenvironmentCancer researchStromal cellImmune systemBiologyMacrophageColorectal cancerCell cultureTumor progressionCellCancer cellCancerImmunologyIn vitro

Abstract

fetched live from OpenAlex

Abstract Tumor-associated macrophages, a major stromal component within the tumor microenvironment (TME), play diverse roles in tumor progression and response to therapy. Although their tumor infiltration is linked to unfavorable prognoses in various cancer types, their specific involvement in colorectal cancer (CRC) remains a subject of debate. Within the TME, macrophages can adopt pro-inflammatory (M1) or immune-suppressive (M2) phenotypes in response to signals. In this study, we aimed to investigate the intricate interplay between CRC cells and macrophages under different tumor microenvironmental stresses, shedding light on the impact of macrophage phenotype and function on tumor cell behavior. We characterized signaling pathways and macrophage markers in the THP-1 monocytic cell line, differentiating THP-1 cells into M0 macrophages and polarizing them into M1 and M2 phenotypes using distinct inducers, LPS+IFNγ or IL4+IL13, respectively. Treatment with M1 and M2 inducers resulted in the induction of p-STAT1 and p-STAT6 signaling, as well as metabolic markers like IDO and TGM2, respectively, in THP-1 cells. Subsequently, we collected conditioned media (CM) from M0, M1, and M2 macrophages and assessed their impact on colon cancer cell proliferation. Consistent with previous studies, M1 CM demonstrated a suppressive effect on the growth of several CRC cell lines, whereas M0 or M2 CM did not elicit a change. Interestingly, we found a few CRC lines where the M1 CM did not reduce cell growth, suggesting that the response to M1 macrophages may be influenced by tumor cell-intrinsic factors. To gain further insights, a high-content imaging-based workflow was utilized for physical co-cultures of macrophage subtypes and CRC cells. Furthermore, we validated our findings using patient-derived tumor organoids to examine the interaction between macrophages and CRC in a more physiologically relevant context. Overall, our systematic exploration provides valuable insights into the complex interplay between macrophage subtypes and the progression of colon cancer. It emphasizes the influence of the tumor immune microenvironment on cancer cell behavior across diverse intrinsic cellular factors. Citation Format: Chun-Te Chiang, Danielle Hixon, Nevart Mooradian, Pratiksha Kshetri, Scott Valena, Roy Lau, Charlie Ambrose, Michael Doche, Reginald Hill, Shannon M. Mumenthaler. Exploring the interplay between macrophage subtypes and colorectal cancer cell growth [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Tumor Immunology and Immunotherapy; 2023 Oct 1-4; Toronto, Ontario, Canada. Philadelphia (PA): AACR; Cancer Immunol Res 2023;11(12 Suppl):Abstract nr A017.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow), Insufficient payload (model declined to judge)
Consensus categoriesInsufficient payload (model declined to judge)
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.307
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0020.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.001
Science and technology studies0.0010.002
Scholarly communication0.0000.000
Open science0.0010.001
Research integrity0.0000.002
Insufficient payload (model declined to judge)0.0020.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.073
GPT teacher head0.373
Teacher spread0.300 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; both teacher heads agree on what is shown here.

Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2023
Admission routes1
Has abstractyes

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