Km. Grigor et al., THE ORIGIN AND BIOLOGY OF CIS CELLS - GENERAL DISCUSSION, APMIS. Acta pathologica, microbiologica et immunologica Scandinavica, 106(1), 1998, pp. 221-224
Participants at the 4th Copenhagen Workshop on Carcinoma in situ and C
ancer of the Testis, representing cell biologists and tumour biologist
s, met together to discuss the similarities and differences between pr
imordial germ cells (PGCs) of the embryo, and the carcinoma in situ (C
IS) stem cell of human testicular germ cell tumours (GCTs). Much has b
een discovered about PGCs in the last 10 years and we still do not kno
w the exact nature of CIS cells. Knowledge of PGCs comes mainly from m
ouse experiments and knowledge of CIS comes from the study of human tu
mours. A mouse model of human GCT would help to investigate the nature
of CIS cells. Grafting mouse male genital ridges into mouse fetal tes
tes results in the development of testicular tissue and the formation
of teratomatous tumour components. Amplification of PGCs in culture is
possible but this results in their transformation into embryonic germ
(EG) cells. CIS cells die by apoptosis if they are isolated, and shor
t-term culture is only possible if the CIS cells are cultured in their
normal environment within seminiferous tubules. It may be possible fo
r CIS cells to differentiate in culture although they cannot be mainta
ined in culture as isolated cells. Human CIS cells are likely to be fo
rmed as a result of in utero factors rather than agents acting on norm
al adult testicular germ cells. EG cells stimulate feeder cells by par
acrine factors but it is not known if these cells produce autocrine fa
ctors.