Inhibition of C3H/He mouse mammary tumor growth by combined treatment with cyclophosphamide and polyadenylic-polyuridylic acid.
Jung Koo Youn, Fanny Lacour, Gilbert Hue
Abstract
Jung Koo Youn, Fanny Lacour, Gilbert Hue
Abstract
The antitumor effect of an immunomodulator, polyadenylic-polyuridylic acid, in combination with cyclophosphamide (CY) was studied in C3H/He mice bearing established mammary tumors. On Day 14 after tumor graft, mice received either CY (90 mg/kg) alone every 2 weeks for a total of four inoculations or alternate weekly inoculations of the same dose of CY and polyadenylic-polyuridylic acid (300 micrograms) or Bacillus Calmette-Guérin (400 micrograms) during 8 consecutive weeks. On Day 170, the following results were obtained. (a) Mice receiving CY alone showed significantly retarded tumor growth; nevertheless, 30 mice of 34 (88%) died of tumor, and only 1 mouse (3%) was tumor free. (b) In mice receiving combined CY and Bacillus Calmette-Guérin, no more significant tumor inhibition was observed than those receiving CY alone. (c) The most significant tumor inhibition was observed in mice receiving combined CY and polyadenylic-polyuridylic acid. Average tumor diameter on Day 63 was one-third (2 mm) of that of mice receiving CY alone (7 mm); 25 mice of 44 (57%) died of tumor; and 11 mice (25%) were tumor free. In in vitro 51Cr release assays using natural killer-sensitive YAC-1 target cells, cytotoxic activity of splenic nonadherent mononuclear cells of the tumor-bearing mice receiving the combined treatment was highly significantly increased. The importance of these findings relative to clinical application is considered.
OpenAlex reports 20 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The antitumor effect of an immunomodulator, polyadenylic-polyuridylic acid, in combination with cyclophosphamide (CY) was studied in C3H/He mice bearing established mammary tumors. On Day 14 after tumor graft, mice received either CY (90 mg/kg) alone every 2 weeks for a total of four inoculations or alternate weekly inoculations of the same dose of CY and polyadenylic-polyuridylic acid (300 micrograms) or Bacillus Calmette-Guérin (400 micrograms) during 8 consecutive weeks. On Day 170, the following results were obtained. (a) Mice receiving CY alone showed significantly retarded tumor growth; nevertheless, 30 mice of 34 (88%) died of tumor, and only 1 mouse (3%) was tumor free. (b) In mice receiving combined CY and Bacillus Calmette-Guérin, no more significant tumor inhibition was observed than those receiving CY alone. (c) The most significant tumor inhibition was observed in mice receiving combined CY and polyadenylic-polyuridylic acid. Average tumor diameter on Day 63 was one-third (2 mm) of that of mice receiving CY alone (7 mm); 25 mice of 44 (57%) died of tumor; and 11 mice (25%) were tumor free. In in vitro 51Cr release assays using natural killer-sensitive YAC-1 target cells, cytotoxic activity of splenic nonadherent mononuclear cells of the tumor-bearing mice receiving the combined treatment was highly significantly increased. The importance of these findings relative to clinical application is considered.
Key concepts: Cyclophosphamide, Mammary tumor, Cytotoxic T cell, Inoculation, In vitro, Ratón, Internal medicine, Chemistry