Unknown

Dataset Information

0

Molecular signatures mostly associated with NK cells are predictive of relapse free survival in breast cancer patients.


ABSTRACT:

Background

Recent observations suggest that immune-mediated tissue destruction is dependent upon coordinate activation of immune genes expressed by cells of the innate and adaptive immune systems.

Methods

Here, we performed a retrospective pilot study to investigate whether the coordinate expression of molecular signature mostly associated with NK cells could be used to segregate breast cancer patients into relapse and relapse-free outcomes.

Results

By analyzing primary breast cancer specimens derived from patients who experienced either 58-116 months (~5-9 years) relapse-free survival or developed tumor relapse within 9-76 months (~1-6 years) we found that the expression of molecules involved in activating signaling of NK cells and in NK cells: target interaction is increased in patients with favorable prognosis.

Conclusions

The parameters identified in this study, together with the prognostic signature previously reported by our group, highlight the cooperation between the innate and adaptive immune components within the tumor microenvironment.

SUBMITTER: Ascierto ML 

PROVIDER: S-EPMC3694475 | biostudies-literature | 2013 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications


<h4>Background</h4>Recent observations suggest that immune-mediated tissue destruction is dependent upon coordinate activation of immune genes expressed by cells of the innate and adaptive immune systems.<h4>Methods</h4>Here, we performed a retrospective pilot study to investigate whether the coordinate expression of molecular signature mostly associated with NK cells could be used to segregate breast cancer patients into relapse and relapse-free outcomes.<h4>Results</h4>By analyzing primary bre  ...[more]

Similar Datasets

2005-02-23 | GSE2034 | GEO
2005-02-22 | E-GEOD-2034 | biostudies-arrayexpress
2007-05-14 | GSE5327 | GEO
| S-ECPF-GEOD-2034 | biostudies-other
| S-EPMC5053746 | biostudies-literature
| S-EPMC6488226 | biostudies-literature
| S-EPMC7927111 | biostudies-literature
| S-EPMC5008315 | biostudies-literature
| S-EPMC7078275 | biostudies-literature
| S-EPMC3303043 | biostudies-literature