Uterine sarcomas are uncommon, representing approx. 5% of all uterine malignancies [
1]. These tumors are often diagnosed in advanced stages and carry an unfavorable prognosis. The final diagnosis is based upon histological and immunohistochemical analyses of tumor tissue obtained by biopsy or surgical excision [
2]. Due to the low incidence of uterine sarcomas, data concerning both molecular mechanisms of their pathogenesis and therapeutic approaches are quite limited and further information is needed. Since uterine sarcomas are rare, they are also not uniformly treated. The mechanisms involved in the tumorigenesis are only in the beginning of being elucidated. Thus, the establishment of
in vivo systems for basic investigations and testing therapeutic approaches in uterine sarcomas is particularly important. Cell lines originating from these malignancies are rare and so are
in vivo systems. The usefulness of some uterine sarcoma cell lines is limited by the fact that the vast majority of them are not tumorigenic in nude mice. This is also the case for cell lines isolated from low grade endometrial stromal sarcomas, e.g., ESS-1 cells [
3]. For some other cell lines details regarding tumorigenicity in nude mice are missing. In a recent publication Kakuno
et al reported the establishment of a new cell line (OMC-9) originated from a human endometrial stromal sarcoma [
4]. According to the authors, these cells are tumorigenic in nude mice and could, therefore, be useful for development of an
in vivo system. Unfortunately, this cell line was not commercially available till now. Since MES-SA cells established by Harker and coauthors are tumorigenic in nude mice, we decided to use them both for
in vitro and for
in vivo experiments in order to test the efficacy of suberoylanilide hydroxamic acid (SAHA; vorinostat).
Vorinostat is a potent inhibitor of HDACs class I and II. These enzymes are responsible for deacetylation of histones and some other proteins and consequently control the expression of different regulatory genes which are responsible for cell growth, proliferation, apoptosis, autophagy and for regulation of other mechanisms involved in the tumor development and growth [
5‐
11]. Our recent data, both published and unpublished, strongly suggest that some HDACs are deregulated in endometrial stromal sarcomas and other uterine tumors of mesenchymal origin [
12,
13]. The therapeutic utility of vorinostat is supported by the fact that it has been recently approved by FDA for therapy of cutaneous T-cell lymphoma. Moreover, vorinostat is used in clinical trials in patients with other solid tumors, such as mesothelioma, medulloblastoma, prostate and thyroid cancer [
14‐
16]. Our
in vitro and
in vivo data suggest that vorinostat is an active drug potentially suitable for targeted treatment of uterine sarcomas.