CD133 expression is not an independent prognostic factor in stage II and III colorectal cancer but may predict the better outcome in patients with adjuvant therapy

被引:21
|
作者
Mia-Jan, Khalilullah [1 ]
Jung, So Young [1 ]
Kim, Ik-Yong [2 ]
Oh, Sung Soo [3 ]
Choi, EunHee [4 ]
Chang, Sei Jin [3 ,5 ]
Kang, Tae Young [1 ]
Cho, Mee-Yon [1 ,6 ]
机构
[1] Yonsei Univ, Wonju Coll Med, Dept Pathol, Wonju, South Korea
[2] Yonsei Univ, Wonju Coll Med, Dept Surg, Wonju, South Korea
[3] Yonsei Univ, Wonju Coll Med, Dept Occupat & Environm Med, Wonju, South Korea
[4] Yonsei Univ, Wonju Coll Med, Inst Lifestyle Med, Wonju, South Korea
[5] Yonsei Univ, Wonju Coll Med, Wonju, South Korea
[6] Yonsei Univ, Wonju Coll Med, Inst Genom Cohort, Wonju, South Korea
关键词
Cancer stem cell; CD133; protein; Human; Colorectal neoplasms; Immunohistochemistry; Chemoradiotherapy; Adjuvant; Prognosis; STEM-CELLS; HEMATOPOIETIC STEM; INITIATING CELLS; POOR-PROGNOSIS; MESSENGER-RNA; MARKER; RESISTANCE; SURVIVAL; LEUKEMIA; PROTEIN;
D O I
10.1186/1471-2407-13-166
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Cancer stem cells (CSCs) are notorious for their capacity of tumor progression, metastasis or resistance to chemo-radiotherapy. However, the undisputed role of cancer stem marker, CD133, in colorectal cancers (CRCs) is not clear yet. Methods: We assessed 271 surgically-resected stage II and III primary CRCs with (171) and without (100) adjuvant therapy after surgery. CD133 expression was analyzed by immunohistochemical (IHC) staining and real-time RT-PCR. CD133 promoter methylation was quantified by pyrosequencing. Results: The CD133 IHC expression was significantly correlated with mRNA expression (p=0.0257) and inversely correlated with the promoter methylation (p=0.0001). CD133 was expressed more frequently in rectal cancer (p=0.0035), and in moderately differentiated tumors (p=0.0378). In survival analysis, CD133 expression was not significantly correlated with overall survival (OS) (p=0.9689) as well as disease-free survival (DFS) (p=0.2103). However, CD133+ tumors were significantly associated with better OS in patients with adjuvant therapy compared to those without adjuvant therapy (p<0.0001, HR 0.125, 95% CI 0.052-0.299). But the patients with CD133-tumors did not show any significant difference of survival according to adjuvant therapy (p=0.055, HR 0.500, 95% CI 0.247-1.015). Conclusions: In stage II and III CRCs, CD133 IHC expression may signify the benefit for adjuvant therapy although it is not an independent prognostic factor.
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页数:10
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