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Contribution of Na + ,HCO 3 − ‐cotransport to cellular pH control in human breast cancer: A role for the breast cancer susceptibility locus NBCn1 (SLC4A7)
Author(s) -
Boedtkjer Ebbe,
Moreira José M.A.,
Mele Marco,
Vahl Pernille,
Wielenga Vera T.,
Christiansen Peer M.,
Jensen Vibeke E.D.,
Pedersen Stine F.,
Aalkjaer Christian
Publication year - 2012
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.27782
Subject(s) - cotransporter , breast cancer , intracellular ph , chemistry , symporter , human breast , endocrinology , intracellular , biology , medicine , transporter , cancer , biochemistry , sodium , gene , organic chemistry
Genome‐wide association studies recently linked the locus for Na + ,HCO 3 − ‐cotransporter NBCn1 (SLC4A7) to breast cancer susceptibility, yet functional insights have been lacking. To determine whether NBCn1, by transporting HCO 3 − into cells, may dispose of acid produced during high metabolic activity, we studied the expression of NBCn1 and the functional impact of Na + ,HCO 3 − ‐cotransport in human breast cancer. We found that the plasmalemmal density of NBCn1 was 20–30% higher in primary breast carcinomas and metastases compared to matched normal breast tissue. The increase in NBCn1 density was similar in magnitude to that observed for Na + /H + ‐exchanger NHE1 (SLC9A1), a transporter previously implicated in cell migration, proliferation and malignancy. In primary breast carcinomas, the apparent molecular weight for NBCn1 was increased compared to normal tissue. Using pH‐sensitive fluorophores, we showed that Na + ,HCO 3 − ‐cotransport is the predominant mechanism of acid extrusion and is inhibited 34 ± 9% by 200 μM 4,4′‐diisothiocyanatostilbene‐2,2′‐disulfonic acid in human primary breast carcinomas. At intracellular pH (pH i ) levels >6.6, CO 2 /HCO 3 − ‐dependent mechanisms accounted for >90% of total net acid extrusion. Na + /H + ‐exchange activity was prominent only at lower pH i ‐values. Furthermore, steady‐state pH i was 0.35 ± 0.06 units lower in the absence than in the presence of CO 2 /HCO 3 − . In conclusion, expression of NBCn1 is upregulated in human primary breast carcinomas and metastases compared to normal breast tissue. Na + ,HCO 3 − ‐cotransport is a major determinant of pH i in breast cancer and the modest DIDS‐sensitivity is consistent with NBCn1 being predominantly responsible. Hence, our results suggest a major pathophysiological role for NBCn1 that may be clinically relevant.