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Research Article

Securin identifies a subgroup of patients with poor outcome in rectal cancer treated with long-course (chemo)radiotherapy

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Pages 1158-1166 | Received 21 Jan 2011, Accepted 08 Apr 2011, Published online: 24 Oct 2011

Figures & data

Table I. The clinical characteristics of the patients in the three groups.

Figure 1. Immunohistochemical staining of securin (a) and Ki-67 (b) in rectal cancer. Staining pattern of Ki-67 was almost exclusively nuclear, while securin had a combination of nuclear and cytoplasmic staining with a clear prominence of nuclear one.

Figure 1. Immunohistochemical staining of securin (a) and Ki-67 (b) in rectal cancer. Staining pattern of Ki-67 was almost exclusively nuclear, while securin had a combination of nuclear and cytoplasmic staining with a clear prominence of nuclear one.

Table II. The expression of securin and Ki-67 in the operative specimens related to key clinicopathological variables.

Table III. The pairwise-comparison of biopsy and operative specimens according to securin and Ki-67 expression.

Figure 2. Securin expression in operative specimens of the long-course (chemo)RT patients related to DFS and DSS (a–b). Tumour regression grade (TRG) after long-course (chemo)RT related to DFS and DSS (c–d).

Figure 2. Securin expression in operative specimens of the long-course (chemo)RT patients related to DFS and DSS (a–b). Tumour regression grade (TRG) after long-course (chemo)RT related to DFS and DSS (c–d).
Supplemental material

http://www.informahealthcare.com/doi/abs/10.3109/0284186X.2011.584327

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