Unique sphingolipid signature identifies luminal and triple‐negative breast cancer subtypes

Author:

Kar Animesh1,Medatwal Nihal2,Rajput Kajal2,Mandal Susmita3,Pani Trishna2,Khan Ali2,Sharma Pankaj2,Oberoi Ajit Singh4,Vishwakarma Gayatri56,Deo SVS4,Jolly Mohit Kumar3,Bajaj Avinash1,Dasgupta Ujjaini2ORCID

Affiliation:

1. Laboratory of Nanotechnology and Chemical Biology, Regional Centre for Biotechnology NCR Biotech Science Cluster Faridabad Haryana India

2. Amity Institute of Integrative Sciences and Health Amity University Haryana Gurgaon Haryana India

3. Centre for BioSystems Science and Engineering Indian Institute of Science Bangalore India

4. Department of Surgical Oncology, BRA‐Institute Rotary Cancer Hospital All India Institute of Medical Sciences New Delhi India

5. Department of Biostatistics Indian Spinal Injuries Centre New Delhi India

6. The George Institute of Global Health New Delhi India

Abstract

AbstractBreast cancer (luminal and triple‐negative breast cancer [TNBC]) is the most common cancer among women in India and worldwide. Altered sphingolipid levels have emerged as a common phenomenon during cancer progression. However, these alterations are yet to be translated into robust diagnostic and prognostic markers for cancer. Here, we present the quantified sphingolipids of tumor and adjacent‐normal tissues from patients of luminal (n = 70) and TNBC (n = 42) subtype from an Indian cohort using targeted liquid chromatography mass spectrometry. We recorded unique sphingolipid profiles that distinguished luminal and TNBC tumors in comparison to adjacent normal tissue by six‐sphingolipid signatures. Moreover, systematic comparison of the profiles of luminal and TNBC tumors provided a unique five‐sphingolipid signature distinguishing the two subtypes. We further identified key sphingolipids that can stratify grade II and grade III tumors of luminal and TNBC subtype as well as their lymphovascular invasion status. Therefore, we provide the right evidence to develop these candidate sphingolipids as widely acceptable marker/s capable of diagnosing luminal vs TNBC subtype of breast cancer, and predicting the disease severity by identifying the tumor grade.

Funder

Indian Council of Medical Research

Science and Engineering Research Board

Douglas Bomford Trust

Publisher

Wiley

Subject

Cancer Research,Oncology

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Sphingomyelin Metabolism Modifies Luminal A Breast Cancer Cell Line under a High Dose of Vitamin C;International Journal of Molecular Sciences;2023-12-08

2. The Effect of Cholesterol in MCF7 Human Breast Cancer Cells;International Journal of Molecular Sciences;2023-03-21

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