𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Comparison of cellular basis of drug sensitivity of human colon, pancreatic, and renal carcinoma cell lines with that of leukemia cell lines

✍ Scribed by Shogo Ozawa; Tetsuya Yasuda; Makoto Inaba


Book ID
104684513
Publisher
Springer
Year
1988
Tongue
English
Weight
682 KB
Volume
22
Category
Article
ISSN
0344-5704

No coin nor oath required. For personal study only.

✦ Synopsis


In an attempt to find how much the low therapeutic effectiveness of antitumor drugs against so-called chemotherapy-refractory tumors such as colon carcinoma depends on drug sensitivity at the cellular level, sensitivity of five carcinoma cell lines (three colorectal, one pancreatic, and one renal) to nine typical anticancer agents was compared in vitro with that of four generally chemotherapy-susceptible leukemia cell lines. Sensitivity was assessed in terms of the percentage cell growth in control cultures, which was determined by exposing exponentially growing cells for 48 h to the following antitumor drugs: 1-(4-amino-2-methylpyridine-5-yl)-methyl-3-(2-chloroethyl)3-nitrosourea hydrochloride (ACNU), adriamycin (ADM), bleomycin (BLM), cisplatin (DDP), etoposide (VP-16), 5-fluorouracil (5FU), mitomycin C (MMC), methotrexate (MTX), and vinblastine (VLB). As expected, 10-fold or greater differences in sensitivity were scarcely ever observed between the two kinds of cell lines. Thus, we recorded a result of more (or less) sensitivity when there was a difference of 3-fold or more; and compared the drug sensitivity in every pair of carcinoma and leukemia cell lines (20 pairs for each drug). We found that carcinoma cell lines were less sensitive to VP-16, ADM, DDP, and MTX than leukemia cell lines in 18, 15, 12, and 10 of 20 pairs, respectively; only one opposite case was observed, with DDP. On the other hand, no such tendency between the two groups was observed with BLM, 5FU, or MMC. Overall, significantly different sensitivities were observed between them in 91 out of 180 pairs (i.e., 9 antitumor drugs x 5 carcinomas x 4 leukemias), and carcinoma cell lines were less sensitive than leukemia cell lines in 79 of these 91 pairs. These results suggest that the refractoriness of colon carcinoma, etc. to chemotherapy is, at least in part, due to low drug sensitivity of the tumor cell itself.


πŸ“œ SIMILAR VOLUMES


In vitro chemotherapy sensitivity patter
✍ M. V. Agrez; M. M. Ames; M. M. Lieber πŸ“‚ Article πŸ“… 1983 πŸ› John Wiley and Sons 🌐 English βš– 306 KB πŸ‘ 1 views

The cells obtained from four established human colon carcinoma cell lines were cultured in soft agar in the presence of eight chemotherapeutic agents that have been used clinically in patients with metastatic colorectal carcinoma. 5-Fluorouracil, mitomycin C , adriamycin, and cis-platinum were highl

CPT-11 in human colon-cancer cell lines
✍ Willy J.M. Jansen; Bas Zwart; Saskia T.M. Hulscher; Giuseppe Giaccone; Herbert M πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 French βš– 104 KB πŸ‘ 2 views

CPT-11, a new semisynthetic derivative of camptothecin, is active in a number of tumor types in the clinic, including colon cancer. CPT-11 is a drug that is converted into the active metabolite SN-38 by a carboxylesterase. Experiments were performed to obtain more insight in the cellular characteris

Clonal heterogeneity of the sensitivity
✍ Guo-Hao K. Zhou; Gwendolyn L. Sechrist; Michael G. Brattain; Kathleen M. Mulder πŸ“‚ Article πŸ“… 1995 πŸ› John Wiley and Sons 🌐 English βš– 907 KB

## Abstract Spontaneously arising, TGFΞ²~1~‐resistant colonies were isolated directly from the soft agarose plates of MOSER human colon carcinoma cells grown in the presence of TGFΞ²~1~ but in the absence of serum. The colonies were cloned by limiting dilution and screened in a monolayer proliferatio