| Literature DB >> 24317739 |
Yoshihiro Kano1, Hideshi Ishii1, Masamitsu Konno1, Makoto Yamasaki2, Hiroshi Miyata2, Shimpei Nishikawa1, Atsushi Hamabe1, Hisataka Ogawa1, Hidekazu Takahashi2, Katsuya Ohta1, Shinichiro Hasegawa1, Kouji Tanaka2, Takahito Fukusumi1, Masahisa Otsuka2, Koichi Kawamoto2, Naotsugu Haraguchi2, Rika Fujimoto3, Masaharu Isobe3, Yasuhiko Tomita4, Nariaki Matsuura5, Shuji Takiguchi2, Masaki Mori2, Yuichiro Doki2.
Abstract
Secondary solid tumors that occur after hematopoietic stem cell transplantation (HSCT) are late complications of HSCT. Previously, secondary solid tumors were considered to be recipient-derived cells because transplanted cells do not contain epithelial cells. Recently, however, not only donor‑derived epithelial cells but also donor-derived secondary solid tumors have also been reported in mice and humans. It means that circulating bone marrow-derived stem cells (BMDCs) including hematopoietic stem cells include the stem cells of many tissue types and the precancerous cells of many solid tumors. In most reports of donor-derived secondary solid tumors, however, tumors contained a low proportion of BMDC-derived epithelial cells in mixed solid tumor tissues. To our knowledge, there are only five known cases of completely donor-derived tumor tissues, i.e., four oral SCCs and a pharyngeal SCC. In this study, we analyzed five human clinical samples of solid tumors, i.e., two esophageal squamous cell carcinomas (SCCs), two oral SCCs and a tongue carcinoma. In the oral and tongue, completely donor-derived tissues were not observed, but in esophagus a completely donor-derived esophageal epidermis and SCC were observed for the first time. In addition, in another esophageal SCC patient, a completely donor-derived dysplasia region of esophageal epidermis was observed near recipient-derived SCC. This study suggests that BMDC-derived cells include the stem cells of esophageal epidermis and the precancerous cells of esophageal SCC and can differentiate into esophageal epithelium and esophageal SCC.Entities:
Mesh:
Year: 2013 PMID: 24317739 DOI: 10.3892/ijo.2013.2206
Source DB: PubMed Journal: Int J Oncol ISSN: 1019-6439 Impact factor: 5.650