An unsupervised MVA method to compare specific regions in human breast tumor tissue samples using ToF-SIMS

Citation

Bluestein, B. M.; Morrish, F.; Graham, D. J.; Guenthoer, J.; Hockenbery, D.; Porter, P. L.; & Gamble, L. J. (2016). An unsupervised MVA method to compare specific regions in human breast tumor tissue samples using ToF-SIMS. Analyst, 141(6), 1947-1957.

Abstract

Imaging time-of-flight secondary ion mass spectrometry (ToF-SIMS) and principal component analysis (PCA) were used to investigate two sets of pre-and post-chemotherapy human breast tumor tissue sections to characterize lipids associated with tumor metabolic flexibility and response to treatment. The micron spatial resolution imaging capability of ToF-SIMS provides a powerful approach to attain spatially-resolved molecular and cellular data from cancerous tissues not available with conventional imaging techniques. Three ca. 1 mm(2) areas per tissue section were analyzed by stitching together 200 mu m x 200 mu m raster area scans. A method to isolate and analyze specific tissue regions of interest by utilizing PCA of ToF-SIMS images is presented, which allowed separation of cellularized areas from stromal areas. These PCA-generated regions of interest were then used as masks to reconstruct representative spectra from specifically stromal or cellular regions. The advantage of this unsupervised selection method is a reduction in scatter in the spectral PCA results when compared to analyzing all tissue areas or analyzing areas highlighted by a pathologist. Utilizing this method, stromal and cellular regions of breast tissue biopsies taken pre- versus post-chemotherapy demonstrate chemical separation using negatively-charged ion species. In this sample set, the cellular regions were predominantly all cancer cells. Fatty acids (i.e. palmitic, oleic, and stearic), monoacylglycerols, diacylglycerols and vitamin E profiles were distinctively different between the pre-and post-therapy tissues. These results validate a new unsupervised method to isolate and interpret biochemically distinct regions in cancer tissues using imaging ToF-SIMS data. In addition, the method developed here can provide a framework to compare a variety of tissue samples using imaging ToF-SIMS, especially where there is section-to-section variability that makes it difficult to use a serial hematoxylin and eosin (H&E) stained section to direct the SIMS analysis.

Keyword(s)

cancer cell-lines
chemotherapy
cluster ion
imaging mass-spectrometry
lipidomic analysis
localization
metabolism
microenvironment
resistance
skeletal-muscle

Notes

Dg7ix
Times Cited:3
Cited References Count:58

Reference Type

Journal Article

Secondary Title

Analyst

Author(s)

Bluestein, B. M.
Morrish, F.
Graham, D. J.
Guenthoer, J.
Hockenbery, D.
Porter, P. L.
Gamble, L. J.

Year Published

2016

Volume Number

141

Issue Number

6

Pages

1947-1957

DOI

10.1039/c5an02406d