Abstract

Breast cancer is estimated to be the leading cancer type among new cases in American women. Core biopsy data have shown a close association between breast hyperplasia and breast cancer. The early diagnosis and treatment of breast hyperplasia are extremely important to prevent breast cancer. The Mongolian medicine RuXian-I is a traditional drug that has achieved a high level of efficacy and a low incidence of side effects in its clinical use. However, for detecting the efficacy of RuXian-I, a rapid and accurate evaluation method based on metabolomic data is still lacking. Therefore, we proposed a framework, named the metabolomics deep belief network (MDBN), to analyze breast hyperplasia metabolomic data. We obtained 168 samples of metabolomic data from an animal model experiment of RuXian-I, which were averaged from control groups, treatment groups, and model groups. In the process of training, unlabelled data were used to pretrain the Deep Belief Networks models, and then labelled data were used to complete fine-tuning based on a limited-memory Broyden Fletcher Goldfarb Shanno (L-BFGS) algorithm. To prevent overfitting, a dropout method was added to the pretraining and fine-tuning procedures. The experimental results showed that the proposed model is superior to other classical classification methods that are based on positive and negative spectra data. Further, the proposed model can be used as an extension of the classification method for metabolomic data. For the high accuracy of classification of the three groups, the model indicates obvious differences and boundaries between the three groups. It can be inferred that the animal model of RuXian-I is well established, which can lay a foundation for subsequent related experiments. This also shows that metabolomic data can be used as a means to verify the effectiveness of RuXian-I in the treatment of breast hyperplasia.

Highlights

  • In Cancer Statistics 2018, breast cancer was identified as the leading cancer type among the estimated new cases, and is the second most frequent type among estimated deaths in American women [1]

  • We evaluated our proposed method, metabolomics deep belief network (MDBN), in the metabolomic dataset

  • We proposed an MDBN to classify the breast hyperplasia (BH) metabolomic data

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Summary

Introduction

In Cancer Statistics 2018, breast cancer was identified as the leading cancer type among the estimated new cases, and is the second most frequent type among estimated deaths in American women [1]. Core biopsy data have shown a close association between breast hyperplasia (BH) and breast cancer (BC) [2]. Breast lesions can be either benign or malignant, and the probability of a lesion being benign is higher. BH is one of the leading causes of breast lesions, and refers to hyperplasia of the mammary epithelium and fibrous tissue, degenerative lesions in the mammary ducts and lobules, and the progressive growth of connective tissue [3,4]. The pathogenesis of BH is mainly due to the imbalance of endocrine hormones. The early diagnosis and treatment of a BH is extremely important

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