Isolation and characterization of a new human breast cancer cell line, KPL-4, expressing the Erb B family receptors and interleukin-6

Citation
J. Kurebayashi et al., Isolation and characterization of a new human breast cancer cell line, KPL-4, expressing the Erb B family receptors and interleukin-6, BR J CANC, 79(5-6), 1999, pp. 707-717
Citations number
36
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
BRITISH JOURNAL OF CANCER
ISSN journal
00070920 → ACNP
Volume
79
Issue
5-6
Year of publication
1999
Pages
707 - 717
Database
ISI
SICI code
0007-0920(199902)79:5-6<707:IACOAN>2.0.ZU;2-T
Abstract
A new human breast cancer cell line, KPL-4, was recently isolated from the malignant pleural effusion of a breast cancer patient with an inflammatory skin metastasis. This cell line can be cultured under serum-free conditions and is tumorigenic in female athymic nude mice. Flow cytometric analysis r evealed the expression of Erb B-1, -2 and -3. Dot blot hybridization showed a 15-fold amplification of the erb B-2. Reverse transcription-polymerase c hain reaction analysis showed a detectable level of mRNA expression of all the Erb B family receptors. in addition, all the receptors were autophospho rylated under a serum-supplemented condition. Unexpectedly, transplanted KP L-4 tumours induced cachexia of recipient mice. A high concentration of int erleukin-6 (IL-6) was detected in both the culture medium and the serum of mice. The weight of tumours significantly correlated with the serum IL-6 le vel. The antiproliferative effect of a humanized anti-Erb B-2 monoclonal an tibody, rhuMAbHER2, was investigated. This antibody significantly inhibited the growth of KPL-4 cells in vitro but modestly in vivo. Loss of mouse bod y weight was partly reversed by rhuMAbHER2. These findings suggest that KPL -4 cells may be useful in the development of new strategies against breast cancer overexpressing the Erb B family receptors and against IL-6-induced c achexia.