AI Article Synopsis

  • Mass spectrometry (MS), particularly MALDI-TOF MS, shows promise in specifically detecting ovarian cancer by analyzing protein patterns in low-concentration cell mixtures.
  • The study focuses on using vaginal lavages from a mouse model of high-grade serous ovarian carcinoma (HGSOC) to monitor disease progression.
  • Findings indicate that specific protein fingerprints in the 4-20 kDa region consistently correlate with cancer progression and are stable across different test subjects.

Article Abstract

Mass spectrometry (MS) offers high levels of specificity and sensitivity in clinical applications, and we have previously been able to demonstrate that matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) MS is capable of distinguishing two-component cell mixtures at low limits of detection. Ovarian cancer is notoriously difficult to detect due to the lack of diagnostic techniques available to the medical community. By sampling a local microenvironment, such as the vaginal canal and cervix, a MS based method is presented for monitoring disease progression from proximal samples to the diseased tissue. A murine xenograft model of high grade serous ovarian carcinoma (HGSOC) was used for this study, and vaginal lavages were obtained from mice on a weekly basis throughout disease progression and subjected to our MALDI-TOF MS workflow followed by statistical analyses. Proteins in the 4-20 kDa region of the mass spectrum yielded a fingerprint that we could consistently measure over time that correlated with disease progression. These fingerprints were found to be largely stable across all mice, with the protein fingerprint converging toward the end point of the study. MALDI-TOF MS serves as a unique analytical technique for measuring a sampled vaginal microenvironment in a specific and sensitive manner for the detection of HGSOC in a murine model.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7020100PMC
http://dx.doi.org/10.1021/acs.jproteome.9b00694DOI Listing

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