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British Journal of Cancer logoLink to British Journal of Cancer
. 1976 Sep;34(3):262–271. doi: 10.1038/bjc.1976.161

The sensitivity of a malignant cell line to hyperthermia (42 degrees C) at low intracellular pH.

J A Dickson, B E Oswald
PMCID: PMC2025171  PMID: 9969

Abstract

The postulate that low intracellular pH acts as a preconditioner for the destructuve effects of hyperthermia (42 degrees C) was examined, using a heat-sensitive line of malignant cells derived from rat mammary gland (SDB). Intracellular pH (pHi) was measured indirectly, from the distribution of the weak, non-metabolizable organic acid 5,5-dimethyl-2,4-oxazolidinedione (DMO) between intra- and extra-cellular water. Respiration, aerobic and anaerobic and anaerobic glycolysis of the cells were studied at normal pHi (pH 7-0-7-4) or at low pHi (pH 6-2-6-6) and at 38 degrees C or 42 degrees C over 6 h in Warburg manometers; the ability of the cells to replicate in culture was examined after 3 h or 6 h incubation in the flasks. The relationship between pHi and extracellular pH (pHe) depended upon the buffer system used and the exact pH in question; no assumption regarding pHi based only on pHe measurement could be made. At 38 degrees C and low pHi, the Pasteur effect became negative due to a relatively greater inhibition of anaerobic than aerobic glycolysis. Respiration was unaffected and cell replicative ability unimpaired. At 42 degrees C and normal pHi, respiration was totally inhibited after 4 h and the Pasteur effect was decreased, in this case due to a compensatory increase in aerobic glycolysis without alteration in anaerobic CO2 production. Low pHi in the presence of hyperthermia enabled cell respiration to continue at a reduced level with no further change in glycolysis. There was delayed cell replication after 3 h at 42 degrees C and inability to multiply following 6 h hyperthermia: low pHi did not influence these results. It is concluded that with these cancer cells, pHi values maintained in the region of 1-0 pH unit below normal for 6 h had no deleterious effect on the cells. No sensitizing effect of the low pHi for the destructive effect of hyperthermia on the cells was observed.

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Selected References

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  1. Bickis I. J., Henderson I. W. Biochemical studies of human tumors. I. Estimation of tumor malignancy from metabolic measurements in vitro. Cancer. 1966 Jan;19(1):89–102. doi: 10.1002/1097-0142(196601)19:1<89::aid-cncr2820190110>3.0.co;2-e. [DOI] [PubMed] [Google Scholar]
  2. Butler T. C., Waddell W. J., Poole D. T. Intracellular pH based on the distribution of weak electrolytes. Fed Proc. 1967 Sep;26(5):1327–1332. [PubMed] [Google Scholar]
  3. Cavaliere R., Ciocatto E. C., Giovanella B. C., Heidelberger C., Johnson R. O., Margottini M., Mondovi B., Moricca G., Rossi-Fanelli A. Selective heat sensitivity of cancer cells. Biochemical and clinical studies. Cancer. 1967 Sep;20(9):1351–1381. doi: 10.1002/1097-0142(196709)20:9<1351::aid-cncr2820200902>3.0.co;2-#. [DOI] [PubMed] [Google Scholar]
  4. Dickson J. A., Ellis H. A. The influence of tumor volume and the degree of heating on the response of the solid Yoshida sarcoma to hyperthermia (40-42 degrees). Cancer Res. 1976 Mar;36(3):1188–1195. [PubMed] [Google Scholar]
  5. Dickson J. A. Letter: Hyperthermia in the treatment of cancer. Cancer Chemother Rep. 1974 May-Jun;58(3):294–296. [PubMed] [Google Scholar]
  6. Dickson J. A., Muckle D. S. Total-body hyperthermia versus primary tumor hyperthermia in the treatment of the rabbit VX-2 carcinoma. Cancer Res. 1972 Sep;32(9):1916–1923. [PubMed] [Google Scholar]
  7. Dickson J. A., Shah D. M. The effects of hyperthermia (42 degrees C) on the biochemistry and growth of a malignant cell line. Eur J Cancer. 1972 Oct;8(5):561–571. doi: 10.1016/0014-2964(72)90110-7. [DOI] [PubMed] [Google Scholar]
  8. Dickson J. A., Suzangar M. A predictive in vitro assay for the sensitivity of human solid tumours to hyperthermia (42 degrees C) and its value in patient management. Clin Oncol. 1976 Jun;2(2):141–155. [PubMed] [Google Scholar]
  9. Dickson J. A., Suzangar M. In vitro-in vivo studies on the susceptibility of the solid Yoshida sarcoma to drugs and hyperthermia (42 degrees). Cancer Res. 1974 Jun;34(6):1263–1274. [PubMed] [Google Scholar]
  10. EDEN M., HAINES B., KAHLER H. The pH of rat tumors measured in vivo. J Natl Cancer Inst. 1955 Oct;16(2):541–556. [PubMed] [Google Scholar]
  11. IYPE P. T., BHARGAVA P. M. THE RESPIRATION OF ISOLATED RAT-HEPATIC CELLS IN SUSPENSION. Biochem J. 1965 Jan;94:284–288. doi: 10.1042/bj0940284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Mondovì B., Strom R., Rotilio G., Finazzi Agrò A., Cavaliere R., Rossi Fanelli A. The biochemical mechanism of selective heat sensitivity of cancer cells. I. Studies on cellular respiration. Eur J Cancer. 1969 May;5(2):129–136. doi: 10.1016/0014-2964(69)90059-0. [DOI] [PubMed] [Google Scholar]
  13. Overgaard K., Overgaard J. Investigations on the possibility of a thermic tumour therapy. I. Short-wave treatment of a transplanted isologous mouse mammary carcinoma. Eur J Cancer. 1972 Feb;8(1):65–78. doi: 10.1016/0014-2964(72)90085-0. [DOI] [PubMed] [Google Scholar]
  14. PATTERSON M. S., GREENE R. C. MEASUREMENT OF LOW ENERGY BETA-EMITTERS IN AQUEOUS SOLUTION BY LIQUID SCINTILLATION COUNTING OF EMULSIONS. Anal Chem. 1965 Jun;37:854–857. doi: 10.1021/ac60226a017. [DOI] [PubMed] [Google Scholar]
  15. Poole D. T. Intracellular pH of the Ehrlich ascites tumour cell as it is affected by sugars and sugar derivatives. J Biol Chem. 1967 Aug 25;242(16):3731–3736. [PubMed] [Google Scholar]
  16. RINALDINI L. M. An improved method for the isolation and quantitative cultivation of embryonic cells. Exp Cell Res. 1959 Mar;16(3):477–505. doi: 10.1016/0014-4827(59)90119-3. [DOI] [PubMed] [Google Scholar]
  17. Robson J. S., Bone J. M., Lambie A. T. Intracellular pH. Adv Clin Chem. 1968;11:213–275. doi: 10.1016/s0065-2423(08)60060-8. [DOI] [PubMed] [Google Scholar]
  18. SCHLOERB P. R., BLACKBURN G. L., GRANTHAM J. J., MALLARD D. S., CAGE G. K. INTRACELLULAR PH AND BUFFERING CAPACITY OF THE WALKER-256 CARCINOMA. Surgery. 1965 Jul;58:5–11. [PubMed] [Google Scholar]
  19. Snow C., Allen A. The release of radioactive nucleic acids and mucoproteins by trypsin and ethylenediaminetetra-acetate treatment of baby-hamster cells in tissue culture. Biochem J. 1970 Oct;119(4):707–714. doi: 10.1042/bj1190707. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. WADDELL W. J., BUTLER T. C. Calculation of intracellular pH from the distribution of 5,5-dimethyl-2,4-oxazolidinedione (DMO); application to skeletal muscle of the dog. J Clin Invest. 1959 May;38(5):720–729. doi: 10.1172/JCI103852. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Waddell W. J., Bates R. G. Intracellular pH. Physiol Rev. 1969 Apr;49(2):285–329. doi: 10.1152/physrev.1969.49.2.285. [DOI] [PubMed] [Google Scholar]
  22. Zieve P. D., Solomon H. M. The intracellular pH of the human platelet. J Clin Invest. 1966 Aug;45(8):1251–1254. doi: 10.1172/JCI105431. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. von Ardenne M. Selective multiphase cancer therapy: conceptual aspects and experimental basis. Adv Pharmacol Chemother. 1972;10:339–380. doi: 10.1016/s1054-3589(08)60527-x. [DOI] [PubMed] [Google Scholar]

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