High Prevalence of Activated Intraepithelial Cytotoxic T Lymphocytes and Increased Neoplastic Cell Apoptosis in Colorectal Carcinomas with Microsatellite Instability
Microsatellite instability (MSI) characterizes colorectal carcinomas (CRCs) in hereditary nonpolyposis colorectal cancer (HNPCC) syndrome and a proportion of sporadic CRCs. These MSI + CRCs share several clinicopathological features, including a reputation for better survival rates than MSI − cases...
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Veröffentlicht in: | The American journal of pathology 1999-06, Vol.154 (6), p.1805-1813 |
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Zusammenfassung: | Microsatellite instability (MSI) characterizes colorectal carcinomas (CRCs) in hereditary nonpolyposis colorectal cancer (HNPCC) syndrome and a proportion of sporadic CRCs. These MSI
+ CRCs share several clinicopathological features, including a reputation for better survival rates than MSI
− cases and a pronounced stromal inflammatory reaction of still undefined nature. In the present study, the presence, spatial distribution, and activation status of infiltrating cytotoxic effectors were investigated comparatively in 18 MSI
+ and 37 MSI
− CRCs by immunohistochemistry. The frequency of apoptosis was also evaluated by morphology and
in situ end-labeling. MSI
+ cases carried significantly higher numbers of cytotoxic lymphocytes infiltrating within neoplastic epithelial structures, as shown by immunostaining for CD3 (15.1 ± 6.2
versus 4.6 ± 4.1,
P < 0.001), CD8 (13 ± 6.4
versus 3.7 ± 3.8,
P < 0.001), and TIA-1 (11.2 ± 6.5
versus1.9 ± 1.7,
P < 0.001). These cytotoxic effectors were globally more activated in MSI
+ than in MSI
− tumors, as revealed by the expression of granzyme B (5.3 ± 4.5
versus 0.6 ± 1.3,
P < 0.001). In MSI
+ CRCs, the number of intraepithelial activated cytotoxic lymphocytes was significantly correlated with the proximal location of the tumor, a poorly differentiated phenotype, and the presence of peritumor lymphoid nodules. Multivariate analysis revealed that MSI was the major determinant of the presence of activated cytotoxic intraepithelial lymphocytes. Moreover, MSI
+ CRCs also showed a significantly higher percentage of tumor cells undergoing apoptotic cell death (4.1 ± 2.1
versus 2.6 ± 1.1,
P < 0.0001, by the TUNEL method), often located in close proximity of activated cytotoxic lymphocytes. These results are consistent with the presence of anti-tumor cytotoxic immune responses in most of MSI
+ CRCs, a phenomenon that may at least in part contribute to the survival advantage ascribed to these patients. |
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ISSN: | 0002-9440 1525-2191 |
DOI: | 10.1016/S0002-9440(10)65436-3 |