Abstract

Cell killing can be achieved in an acidic environment in tissue culture (medium pH less than 7.0) by agents (nigericin, carbonylcyanide-3-chlorophenylhydrazone (CCCP)) which transport protons from the extracellular space into the cytoplasm. Cell killing is enhanced when these agents are used in combination with compounds (amiloride, 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid (DIDS)) which inhibit the membrane-based exchangers responsible for the regulation of intracellular pH (pHi). We describe experiments which assess the ability of these agents to kill tumour cells in spheroids and in vivo. Both nigericin and CCCP were observed to penetrate tissue based on their ability to kill tumour cells in spheroids. The mean extracellular pH (pHe) of the KHT fibrosarcoma and the EMT-6 sarcoma were observed to be 0.21 and 0.32 pH units more acidic than the mean pHe in muscle tissue. Intraperitoneal (i.p.) administration of the vasodilator hydralazine (10 mg kg-1) caused a reduction of the mean pHe of the KHT but not the EMT-6 tumour. Nigericin (2.5 mg kg-1, i.p.) plus amiloride (10 mg kg-1, i.p.) followed 30 min later by hydralazine (10 mg kg-1, i.p.) reduced the surviving fraction of cells in the KHT and EMT-6 tumours, but had minimal effects on growth delay. When KHT tumours were treated with 15 Gy X-rays followed immediately by nigericin plus amiloride and hydralazine a reduced surviving fraction as well as an increase in tumour growth delay was observed compared to radiation alone. The administration of nigericin (2.5 mg kg-1, i.p.) or the combination of nigericin (2.5 mg kg-1, i.p.) followed by hydralazine (10 mg kg-1, intravenous (i.v.)) resulted in reductions of tumour pHi of 0.27 and 0.29 pH units respectively as determined by 31P magnetic resonance spectroscopy (MRS). Our results show that the combination of nigericin and hydralazine (with or without amiloride) can kill cells in rodent solid tumours and that cell killing is associated with a reduction in the mean pHi of tumour cells.

Highlights

  • Intracellular pH in solid tumours has been observed to have a wider range than that in normal tissue but median pHi (7.2) does not appear to be significantly lower in solid tumours as compared to normal tissue (Vaupel et al, 1989). Taken together these results indicate that cells in solid tumours are surrounded by an acidic extracellular fluid and that tumour cells are actively regulating their pHi to physiological levels

  • After 4 days cell aggregates were transferred into spinner flasks containing 200 ml of a-minimum essential medium (a-MEM) minus bicarbonate supplemented with 25 mM hydroxyethylpiperazine-N'-2-ethanesulfonic acid (Hepes), 10% foetal bovine serum (FBS) and 0.1 mg ml-' kanamycin

  • EMT-6 spheroids were exposed to concentrations of CCCP (1I5pM) and nigericin (3.4,UM) which had been shown previously to be toxic to single cell suspensions (Rotin et al, 1987; Newell & Tannock, 1989)

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Summary

Objectives

The objective of the present study was to determine if agents which produce intracellular acidification and are selectively toxic at low pHe in vitro have anti-tumour effects against two murine transplantable tumours

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