Dose response and growth rates of subcutaneous tumors induced with 3-methylcholanthrene in mice and timing of tumor origin.

نویسندگان

  • H Tanooka
  • K Tanaka
  • H Arimoto
چکیده

The dose response of tumor induction after single s.c. injections of 3-methylcholanthrene (MC) into the groin of mice and the growth rates of the tumors formed were examined. The dose-response curve of tumor induction appeared to be linear at low doses of MC. Analysis of 182 sarcomas produced between 50 and 400 days after MC injection into WB and C3H/He mice, together with previous data on ICR/JCL mice, showed that there was no correlation between the volume-doubling time of tumors and the length of time before tumor appearance or the dose of carcinogen applied. The overall average volume-doubling time of sarcomas in the three strains of mice was 2.6 days. Assuming that a tumor originates from a single cell and that its growth rate before its appearance is constant, individual growth curves were extrapolated to the time of origin of each tumor. Histograms of the distribution of times of origin of tumors showed peaks at about 50 days after application of carcinogen. A one-hit and possibly two-stage type of tumor induction with MC is proposed.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

The effect of steriods on methylcholanthrene-induced subcutaneous tumors in C3H and BALB/c mice.

Tumors were induced in mice with 20-methylcholanthrene for the purpose of studying the anti-cancer activity of steroids. Repeated subcutaneous injections of 20-methylcholanthrene (MC) were used to induce sarcomas in two strains of mice, BALB/c males and CSH/Jax females. Over 80 per cent of the BALB/c and 100 per cent of the C3H mice developed tumors within 90 days after the start of carcinogen ...

متن کامل

Predominance of a cell population less sensitive to carcinogenesis in neoplastic cells of 3-methylcholanthrene-induced tumors in mouse aggregation chimeras.

Tumors were induced by i.m. injections of 3-methylcholanthrene (0.5 mg) in 100% experimental aggregation chimeras derived from two mouse strains C57Bl/6J (hereafter called B6) and A/J, dimorphic for the enzyme glucosephosphate isomerase (Gpi-1a or Gpi-1b) and differing in coat color, aryl hydrocarbon hydroxylase inducibility, and cytotoxic activities of natural killer cells and macrophages. In ...

متن کامل

Treatment of Colon Carcinoma Tumors by Electrolysis: Effect of Electrical Dose and Polarity

Introduction: As a physical treatment, electrochemical therapy (ECHT) has provided an effective and useful  approach  for  treating  localized  tumors.  The  chemical  changes  due  to  a  direct  electric  current  destroy  the  tumor. This study evaluates the effect of electrical dose and polarity on the efficacy of the treatment of a  colon tumor model.  Materials and Methods: In order to in...

متن کامل

Induction of micronuclei in a transplantable murine tumor after multimodality treatment with cis-platin, radiation and hyperthermia

Background: Tumor response after multimodality treatment using combination of radiation, chemotherapeutic drugs and hyperthermia usually assessed by parameters such as tumor growth delay, volume doubling time and regression response. The study herein was conducted to investigate the usefulness of micronucleus assay for assessing the multimodality treatment. Materials and Methods: The ...

متن کامل

Triple tandem mimotope peptide of Epidermal Growth Factor Receptor displaying on the surface of M13 phage induces anti-tumor response in mice tumor model

Introduction: Epidermal growth factor receptor (EGFR) has been shown to play a critical role in tumor cell growth and its overexpression has been observed in many epithelial tumors. In the field of cancer vaccine research, displaying the peptide mimotope on the surface of phage particles has shown promising results. Methods: In this study using m13-PVIII phage display system, two constructs we...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Cancer research

دوره 42 11  شماره 

صفحات  -

تاریخ انتشار 1982