Evidence map›Paper›PMID 29965974›Full record

ArticlePloS one2018

Differential expression and function of CAIX and CAXII in breast cancer: A comparison between tumorgraft models and cells.

Zhijuan Chen, Lingbao Ai, Mam Y Mboge, Chingkuang Tu, Robert McKenna, Kevin D Brown, Coy D Heldermon, Susan C Frost

Expression of concernOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It carries an expression of concern. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

40 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
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  5. Tumor Hypoxia: How Conventional Histology Is Reshaped in Breast Carcinoma.International journal of molecular sciences · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Zhijuan ChenThe Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America.
Lingbao AiThe Department of Medicine, University of Florida, Gainesville, FL, United States of America.
Mam Y MbogeThe Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America.
Chingkuang TuThe Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America.
Robert McKennaThe Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America.
Kevin D BrownThe Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America.
Coy D HeldermonThe Department of Medicine, University of Florida, Gainesville, FL, United States of America.
Susan C FrostThe Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States of America.ORCID 0000-0002-2020-097X
University of Florida · US

Funding

Carbonic anhydrase and pH control in breast cancer cellsR01CA165284 · NCI · UNIVERSITY OF FLORIDA · PI FROST, SUSAN COOKE · 2013 to 2017
$1.7M
NCI NIH HHS R01 CA165284
6 · The paper itself

Abstract

Carbonic anhydrase IX (CAIX) and XII (CAXII) are transmembrane proteins that are associated with cancer progression. We have previously described the catalytic properties of CAIX in MDA-MB-231 breast cancer cells, a line of cells that were derived from a patient with triple negative breast cancer. We chose this line because CAIX expression in breast cancer is a marker of hypoxia and a prognosticator for reduced survival. However, CAXII expression is associated with better survival statistics than those patients with low CAXII expression. Yet CAIX and CAXII have similar catalytic activities. Here we compare the potential roles of CAIX and CAXII in the context of TNBC and estrogen receptor (ER)-positive breast cancer. In tumor graft models, we show that CAIX and CAXII exhibit distinct expression patterns and non-overlapping. We find the same pattern across a panel of TNBC and luminal breast cancer cell lines. This affords an opportunity to compare directly CAIX and CAXII function. Our data suggest that CAIX expression is associated with growth potentiation in the tumor graft model and in a TNBC line using knockdown strategies and blocking activity with an impermeant sulfonamide inhibitor, N-3500. CAXII was not associated with growth potentiation. The catalytic activities of both CAIX and CAXII were sensitive to inhibition by N-3500 and activated at low pH. However, pH titration of activity in membrane ghosts revealed significant differences in the catalytic efficiency and pKa values. These features provide evidence that CAIX is a more efficient enzyme than CAXII at low pH and that CAIX shifts the equilibrium between CO2 and bicarbonate in favor of CO2 production by consuming protons. This suggests that in the acidic microenvironment of tumors, CAIX plays a role in stabilizing pH at a value that favors cancer cell survival.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBiomarkers, TumorBreast NeoplasmsCarbonic Anhydrase IXCarbonic AnhydrasesCatalysisCell Line, TumorCell ProliferationDisease Models, AnimalEnzyme ActivationFemaleGene Knockdown TechniquesHeterograftsHumansHydrogen-Ion ConcentrationBiomarkers, TumorCarbonic Anhydrase IXCarbonic Anhydrases

Identifiers

PMID29965974
PMCPMC6028082
OpenAlexW2810774065

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.