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Learning to Predict Relapse In Invasive Ductal Carcinomas based on the Subcellular Localization of Junctional Proteins

Purpose: The complexity of breast cancer biology makes it challenging to analyze large datasets of clinicopathologic and molecular attributes, towards identifying the key prognostic features and producing systems capable of predicting which patients are likely to relapse. We applied machine learning techniques to analyze a set of well-characterized primary breast cancers, which specified the abundance and localization of various junctional proteins. We hypothesized that disruption of junctional complexes would lead to the cytoplasmic/nuclear redistribution of the protein components and their potential interactions with growth regulating molecules, which would promote relapse, and that machine learning techniques could use the subcellular locations of these proteins, together with standard clinicopathological data, to produce an efficient prognostic classifier. Experimental Design: We used immunohistochemistry to assess the expression and subcellular distribution of 6 junctional proteins, in addition to a panel of 8 standard clinical features and concentrations of 4 "Growth Regulating" proteins, to produce a database involving 36 features, over 66 primary invasive ductal breast carcinomas. A machine learning system was applied to this clinico-pathologic dataset to produce a decision-tree classifier that could predict whether a novel breast cancer patient would relapse. Results: We show that this decision-tree classifier, which incorporates a combination of only 4 features (nuclear a- and b-catenin levels, the total level of PTEN and the number of involved axillary lymph nodes), is able to correctly classify patient outcomes essentially 80% of the time. Further, this classifier is significantly better than classifiers based on any subgroup of these 36 features. Conclusion: This study demonstrates that autonomous machine learning techniques are able to generate simple and efficient decision-tree prognostic classifiers from a wide variety of clinical, pathologic, and biomarker data, and unlike other analytic methods, suggest testable biologic relationships among explicitly identified key variables. The decision-tree classifier resulting from these analytic methods is sufficiently simple and should be widely applicable to a spectrum of clinical cancer settings. Further, the subcellular distribution of junctional proteins, which influences growth regulatory pathways involved in locoregional and metastatic relapse of breast cancer, helped to identify which patients would relapse while their total concentration did not. This emphasizes the need to evaluate the subcellular distribution of junctional proteins in assessing their contribution to tumor progression.

Citation

N. Asgarian, X. Hu, Z. Aktary, K. Chapman, L. Lam, R. Chibbar, J. Mackey, R. Greiner, M. Pasdar. "Learning to Predict Relapse In Invasive Ductal Carcinomas based on the Subcellular Localization of Junctional Proteins". Breast Cancer Research and Treatment, 121(2), pp 527, May 2010.

Keywords: Catenin, cadherin, breast cancer, relapse, PTEN, machine learning, medical informatics, bioinformatics
Category: In Journal
Web Links: Journal entry
  DOI

BibTeX

@article{Asgarian+al:BCRT10,
  author = {Nasimeh Asgarian and Xiuying Hu and Zackie Aktary and Kimberly Ann
    Chapman and Le Lam and Rajni Chibbar and John Mackey and Russ Greiner and
    Manijeh Pasdar},
  title = {Learning to Predict Relapse In Invasive Ductal Carcinomas based on
    the Subcellular Localization of Junctional Proteins},
  Volume = "121",
  Number = "2",
  Pages = {527},
  journal = {Breast Cancer Research and Treatment},
  year = 2010,
}

Last Updated: September 07, 2021
Submitted by Russ Greiner

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