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Record W2507829349 · doi:10.1158/1557-3125.advbc-a097

Abstract A097: Inhibition of the Na+/H+ exchanger (NHE1) increases susceptibility to paclitaxel in invasive breast cancer cells

2013· article· en· W2507829349 on OpenAlexaffabout
Schammim Ray Amith, Jodi Marie Wilkinson, Larry Fliegel

Bibliographic record

VenueMolecular Cancer Research · 2013
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicIon Transport and Channel Regulation
Canadian institutionsUniversity of Alberta
Fundersnot available
KeywordsPaclitaxelCancer researchCell growthChemistryTumor microenvironmentCell cultureCancer cellCancerHomeostasisIntracellular pHPharmacologyCell biologyBiologyBiochemistryMedicineInternal medicineTumor cellsIntracellular

Abstract

fetched live from OpenAlex

Abstract The pH gradient in normal cells is tightly controlled by the activity of various pH regulatory membrane proteins including the Na+/H+ exchanger, NHE1. NHE1 becomes constitutively active in a neoplastic milieu, dysregulating pH homeostasis and altering the survival, differentiation, and proliferation of cells, thus causing them to become tumorigenic. In breast cancer cells, cytoplasmic alkalinization as a result of NHE1 hyper-activity results in an acidic tumor microenvironment that facilitates aggressive cellular proliferation, migration, and invasion leading to tumor metastasis. The pathophysiological role of NHE1 in tumor progression with regards to ion flux is well known, however, the manipulation of pH in and around tumor cells has only recently been considered as a strategy in augmenting cancer therapy. We studied the effect of NHE1 inhibitors EMD87580 ((2-methyl-4,5-di-(methylsulfonyl)-benzoyl)-guanidine) and HMA (5-(N, N-hexamethylene)-amiloride), either alone or in combination with paclitaxel (Taxol), on NHE1 exchanger activity, cell viability, proliferation, migration, and invasive potential, in a highly invasive breast cancer cell line MDA MB 231. We found that cells treated with EMD or HMA in combination with paclitaxel at low doses (0.1nM to 1nM), were significantly more susceptible to cell death than cells treated with paclitaxel or inhibitors alone. While no discernible differences between treatments were observed in cell proliferation rates, a significant reduction in the rate of migration and invasion was observed in cells treated with paclitaxel and either EMD or HMA. To highlight the importance of NHE1 function, we also generated an MDA-MB-231NHE1- knockout cell line for comparison with the wild-type cells that endogenously express NHE1. The NHE1 knockout cell line showed no demonstrable Na+/H+ exchange activity, and much lower rates of proliferation, migration and invasion compared to wild-type cells. Our results demonstrate, for the first time, that inhibition of NHE1 potentially increases the susceptibility of invasive breast cancer cells to paclitaxel-mediated cell death at doses much lower than the established IC50 of paclitaxel in MDA MB 231 cells. Since pH regulation appears to play an integral role in the switch from a normal to a neoplastic microenvironment, these data lend further credence to the importance of NHE1 as a potential target in breast cancer chemotherapy. Supported by the Canadian Breast Cancer Foundation. Citation Format: Schammim Ray Amith, Jodi Marie Wilkinson, Larry Fliegel. Inhibition of the Na+/H+ exchanger (NHE1) increases susceptibility to paclitaxel in invasive breast cancer cells. [abstract]. In: Proceedings of the AACR Special Conference on Advances in Breast Cancer Research: Genetics, Biology, and Clinical Applications; Oct 3-6, 2013; San Diego, CA. Philadelphia (PA): AACR; Mol Cancer Res 2013;11(10 Suppl):Abstract nr A097.

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)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
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 score0.246
Threshold uncertainty score0.990

Codex and Gemma teacher scores by category

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

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 head0.025
GPT teacher head0.314
Teacher spread0.288 · 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; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
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
Published2013
Admission routes2
Has abstractyes

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