Hasegawa Tomonori, Nakashiro Koh-Ichi, Fukumoto Chonji, Hyodo Toshiki, Sawatani Yuta, Shimura Michiko, Kamimura Ryouta, Kuribayashi Nobuyuki, Fujita Atsushi, Uchida Daisuke, Kawamata Hitoshi
Department of Oral and Maxillofacial Surgery, Dokkyo Medical University School of Medicine, Tochigi 321-0293, Japan.
Department of Oral and Maxillofacial Surgery, Ehime University Graduate School of Medicine, Ehime 791-0295, Japan.
Oncol Lett. 2021 Feb;21(2):170. doi: 10.3892/ol.2021.12431. Epub 2021 Jan 4.
Molecules that demonstrate a clear association with the aggressiveness of oral squamous cell carcinoma (OSCC) have not yet been identified. The current study hypothesized that tumor cells in OSCC have three different origins: Epithelial stem cells, oral tissue stem cells from the salivary gland and bone marrow (BM) stem cells. It was also hypothesized that carcinomas derived from less-differentiated stem cells have a greater malignancy. In the present study, sex chromosome analysis by fluorescence hybridization and/or microdissection PCR was performed in patients with OSCC that developed after hematopoietic stem cell transplantation (HSCT) from the opposite sex. OSCC from 3 male patients among the 6 total transplanted patients were considered to originate from donor-derived BM cells. A total of 2/3 patients had distant metastasis, resulting in a poor prognosis. In a female patient with oral potentially malignant disorder who underwent HSCT, there were 10.7% Y-containing cells in epithelial cells, suggesting that some epithelial cells were from the donor. Subsequently, gene expression patterns in patients with possible BM stem cell-derived OSCC were compared with those in patients with normally developed OSCC by microarray analysis. A total of 3 patients with BM stem cell-derived OSCC exhibited a specific pattern of gene expression. Following cluster analysis by the probes identified on BM stem cell-derived OSCC, 2 patients with normally developed OSCC were included in the cluster of BM stem cell-derived OSCC. If the genes that could discriminate the origin of OSCC were identified, OSCCs were classified into the three aforementioned categories. If diagnosis can be performed based on the origin of the cancer cells, a more specific therapeutic strategy may be implemented to improve prognosis. This would be a paradigm shift in diagnostic and therapeutic strategies for OSCC.
尚未确定与口腔鳞状细胞癌(OSCC)侵袭性有明确关联的分子。当前研究假设OSCC中的肿瘤细胞有三种不同起源:上皮干细胞、唾液腺口腔组织干细胞和骨髓(BM)干细胞。还假设源自分化程度较低干细胞的癌具有更高的恶性程度。在本研究中,对接受异性造血干细胞移植(HSCT)后发生OSCC的患者进行了荧光杂交和/或显微切割PCR的性染色体分析。6例移植患者中有3例男性患者的OSCC被认为源自供体来源的BM细胞。总共2/3的患者发生了远处转移,预后较差。在一名接受HSCT的口腔潜在恶性疾病女性患者中,上皮细胞中有10.7%的含Y细胞,表明一些上皮细胞来自供体。随后,通过微阵列分析比较了可能由BM干细胞衍生的OSCC患者与正常发生OSCC患者的基因表达模式。共有3例由BM干细胞衍生的OSCC患者表现出特定的基因表达模式。通过在由BM干细胞衍生的OSCC上鉴定的探针进行聚类分析后,2例正常发生OSCC的患者被纳入由BM干细胞衍生的OSCC聚类中。如果能够鉴定出可区分OSCC起源的基因,OSCC可分为上述三类。如果能够基于癌细胞的起源进行诊断,可能会实施更具针对性的治疗策略以改善预后。这将是OSCC诊断和治疗策略的范式转变。