4.7 Article

Non-small cell lung cancer is characterized by dramatic changes in phospholipid profiles

期刊

INTERNATIONAL JOURNAL OF CANCER
卷 137, 期 7, 页码 1539-1548

出版社

WILEY
DOI: 10.1002/ijc.29517

关键词

non-small cell lung cancer; lipidomics; phospholipids; mass spectrometry; 2D-imaging MS

类别

资金

  1. EU FP7 [Canceralia EU-259737]
  2. Research Foundation-Flanders (FWO) [G.0691.12]
  3. KU Leuven [GOA/11/2009]
  4. Foundation Fournier Majoie (FFM)
  5. Stichting tegen Kanker [F/2014/324]
  6. Agency for Innovation by Science and Technology IWT-Flanders
  7. Olle Engkvist foundation (Sweden)
  8. National Institutes of Health [NIH/NIGMS R01 GM058008-14, NIH/NIGMS P41 GM103391-03]

向作者/读者索取更多资源

Non-small cell lung cancer (NSCLC) is the leading cause of cancer death globally. To develop better diagnostics and more effective treatments, research in the past decades has focused on identification of molecular changes in the genome, transcriptome, proteome, and more recently also the metabolome. Phospholipids, which nevertheless play a central role in cell functioning, remain poorly explored. Here, using a mass spectrometry (MS)-based phospholipidomics approach, we profiled 179 phospholipid species in malignant and matched non-malignant lung tissue of 162 NSCLC patients (73 in a discovery cohort and 89 in a validation cohort). We identified 91 phospholipid species that were differentially expressed in cancer versus non-malignant tissues. Most prominent changes included a decrease in sphingomyelins (SMs) and an increase in specific phosphatidylinositols (PIs). Also a decrease in multiple phosphatidylserines (PSs) was observed, along with an increase in several phosphatidylethanolamine (PE) and phosphatidylcholine (PC) species, particularly those with 40 or 42 carbon atoms in both fatty acyl chains together. 2D-imaging MS of the most differentially expressed phospholipids confirmed their differential abundance in cancer cells. We identified lipid markers that can discriminate tumor versus normal tissue and different NSCLC subtypes with an AUC (area under the ROC curve) of 0.999 and 0.885, respectively. In conclusion, using both shotgun and 2D-imaging lipidomics analysis, we uncovered a hitherto unrecognized alteration in phospholipid profiles in NSCLC. These changes may have important biological implications and may have significant potential for biomarker development. What's new? Cellular membranes are subject to extensive modification in cancer, often with marked alterations in phospholipid metabolism. The extent and nature of those changes are not fully known, however, particularly for non-small cell lung cancer (NSCLC). In this study, lipidomics analysis of phospholipid profiles uncovered dramatic differences between NSCLC and normal lung tissue. The differences were confirmed via 2D-imaging lipidomics in tissue sections. Lipid markers capable of discriminating between tumor and normal tissue and between different NSCLC subtypes were identified. The observed alterations in NSCLC phospholipid profiles may be biologically significant.

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Record, David Reeves, Allyson Ricarte, Ana Rodriguez-Soto, Alexander Ropelewski, Jean Rosario, Morla-Adames Roselkis, David Rowe, Tarun Kanti Roy, Matt Ruffalo, Nancy Ruschman, Angela Sabo, Nina Sachdev, Sinem Saka, Diane Salamon, Pinaki Sarder, Hiroshi Sasaki, Rahul Satija, Diane Saunders, Riley Sawka, Kevin Schey, Heidi Schlehlein, David Scholten, Sarah Schultz, Lauren Schwartz, Melissa Schwenk, Robin Scibek, Ayellet Segre, Matthew Serrata, Walter Shands, Xiaotao Shen, Jay Shendure, Holly Shephard, Lingyan Shi, Tujin Shi, Dong-Guk Shin, Bill Shirey, Max Sibilla, Michal Silber, Jonathan Silverstein, Derek Simmel, Alan Simmons, Dhruv Singhal, Santhosh Sivajothi, Thomas Smits, Francesca Soncin, Qi Song, Valentina Stanley, Tim Stuart, Hanquan Su, Pei Su, Xin Sun, Christine Surrette, Hannah Swahn, Kai Tan, Sarah Teichmann, Abhiroop Tejomay, George Tellides, Kathleen Thomas, Tracey Thomas, Marissa Thompson, Hua Tian, Leonoor Tideman, Cole Trapnell, Albert G. Tsai, Chia-Feng Tsai, Leo Tsai, Elizabeth Tsui, Tina Tsui, Jason Tung, Morgan Turner, Jackie Uranic, Eeshit Dhaval Vaishnav, Sricharan Reddy Varra, Vasyl Vaskivskyi, Dusan Velickovic, Marija Velickovic, Jamie Verheyden, Jessica Waldrip, Douglas Wallace, Xueyi Wan, Allen Wang, Fusheng Wang, Meng Wang, Shuoshuo Wang, Xuefei Wang, Clive Wasserfall, Leonard Wayne, James Webber, Griffin M. Weber, Bei Wei, Jian-Jun Wei, Annika Weimer, Joel Welling, Xingzhao Wen, Zishen Wen, MacKenzie Williams, Seth Winfree, Nicholas Winograd, Abashai Woodard, Devin Wright, Fan Wu, Pei-Hsun Wu, Qiuyang Wu, Xiaodong Wu, Yi Xing, Tiangyang Xu, Manxi Yang, Mingyu Yang, Joseph Yap, Dong Hye Ye, Peng Yin, Zhou Yuan, Chi (Jina) Yun, Ali Zahraei, Kevin Zemaitis, Bo Zhang, Caibin Zhang, Chenyu Zhang, Chi Zhang, Kun Zhang, Shiping Zhang, Ted Zhang, Yida Zhang, Bingqing Zhao, Wenxin Zhao, Jia Wen Zheng, Sheng Zhong, Bokai Zhu, Chenchen Zhu, Diming Zhu, Quan Zhu, Ying Zhu

Summary: The Human BioMolecular Atlas Program (HuBMAP) presents its production phase: the generation of spatial maps of functional tissue units across organs from diverse populations and the creation of tools and infrastructure to advance biomedical research.

NATURE CELL BIOLOGY (2023)

Article Oncology

Anal cancer screening results from 18-to-34-year-old men who have sex with men living with HIV

Yuxin Liu, Swati Bhardwaj, Keith Sigel, John Winters, Joseph Terlizzi, Michael M. Gaisa

Summary: This study investigated the prevalence and severity of anal HPV disease among MSM LWH under the age of 35, finding a high prevalence of HPV infection and precancer but no cases of invasive anal cancer. This supports the adoption of age-based anal cancer screening for this population.

INTERNATIONAL JOURNAL OF CANCER (2024)