The effectiveness of short-term versus long-term exposures to Photofrin II in killing light-activated tumor cells

• Published in: Radiation research Vol. 128; no. 1; p. 82
• Main Authors: Chapman, J D, Stobbe, C C, Arnfield, M R, Santus, R, McPhee, M S
• Format: Journal Article
• Language: English
• Published: United States 01.10.1991
• Subjects: Animals; Cell Death - drug effects; Cell Death - radiation effects; Dihematoporphyrin Ether; Dose-Response Relationship, Drug; Dose-Response Relationship, Radiation; Hematoporphyrins - pharmacology; Light; Mice; Time Factors; Tumor Cells, Cultured - drug effects; Tumor Cells, Cultured - radiation effects
• ISSN: 0033-7587
• DOI: 10.2307/3578070

Asynchronous populations of mouse EMT-6 tumor cells were exposed to various doses of 630-nm light in slowly stirred aerobic suspensions after both short-term and long-term exposures to Photofrin II. All survival curves are characterized by a "threshold" light dose below which no cell inactivation occurs followed by a steep light-dose response. Both the shoulder widths and the inactivation curve slopes are functions of Photofrin II concentration. After high doses of light where survival levels are 0.003 and lower, "resistant tails" are observed on some survival curves. Light doses required to inactivate 50% of tumor cell populations were obtained from whole survival curves and their reciprocals (1/D50% survival) used as inactivation "rates". The amount of Photofrin II within cells was measured by a fluorescence assay. Per unit of fluorescence, this photosensitizer is at least 10 times more effective after long-term than after short-term exposures. After long-term exposures, both fluorescence activity and photosensitizing effectiveness are retained in washed cells for several hours. After short-term exposures, a majority of both the fluorescence and photosensitizing activity is lost by multiple washings or stirring in tissue culture medium without drug. These data suggest that the cellular compartments associated with photosensitization after short-term exposures to Photofrin II are probably different from the cellular compartments associated with photosensitization after long-term exposures to the drug. The data are consistent with known properties of the monomeric and oligomeric components of Photofrin II.