4.7 Article

Clinicopathologic and Prognostic Association of GRP94 Expression in Colorectal Cancer with Synchronous and Metachronous Metastases

Journal

Publisher

MDPI
DOI: 10.3390/ijms22137042

Keywords

GRP94; tumor-infiltrating lymphocyte; colorectal cancer; prognosis

Funding

  1. Bio & Medical Technology Development Program of the National Research Foundation - Korean government [NRF2019M3E5D5065844, 2020M3A9I2107093]
  2. National Research Foundation of Korea [2020M3A9I2107093] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The study evaluated the clinicopathological relevance of GRP94 expression in patients with advanced colorectal cancer with distant metastases. Results showed that high GRP94 expression was more common in patients with a higher density of CD4+ TILs in the synchronous metastases group and served as an independent prognostic factor only in this group.
Patients with advanced colorectal cancer (CRC) with distant metastases have a poor prognosis. We evaluated the clinicopathological relevance of GRP94 expression in these cases. The immunohistochemical expression of GRP94 was studied in 189 CRC patients with synchronous (SM; n = 123) and metachronous metastases (MM; n = 66), using tissue microarray; the association between GRP94 expression, outcome, and tumor-infiltrating lymphocytes (TILs) was also evaluated. GRP94 was expressed in 64.6% (122/189) patients with CRC; GRP94 positivity was found in 67.5% and 59.1% patients with SM and MM, respectively. In the SM group, high GRP94 expression was more common in patients with a higher density of CD4+ TILs (p = 0.002), unlike in the MM group. Survival analysis showed that patients with GRP94 positivity had significantly favorable survival (p = 0.030); after multivariate analysis, GRP94 only served as an independent prognostic factor (p = 0.034; hazard ratio, 0.581; 95% confidence interval, 0.351-0.961) in the SM group. GRP94 expression was detected in 49.4% of metastatic sites and showed significant heterogeneity between primary and metastatic lesions (p = 0.012). GRP94 is widely expressed in CRC with distant metastases; its expression was associated with favorable prognosis in the SM group, unlike in the MM group.

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