Spatial Transcriptomic Analysis of Pituitary Corticotroph Tumors

Author:

Piña Jeremie Oliver12,Faucz Fabio R34,Padilla Cameron34,Floudas Charalampos S5ORCID,Chittiboina Prashant6ORCID,Quezado Martha7,Tatsi Christina84ORCID

Affiliation:

1. Section on Craniofacial Genetic Disorders , Eunice Kennedy Shriver , Bethesda, MD 20892 , USA

2. National Institute of Child Health, and Human Development, National Institutes of Health , Eunice Kennedy Shriver , Bethesda, MD 20892 , USA

3. Molecular Genomics Core , Eunice Kennedy Shriver , Bethesda, MD 20892 , USA

4. National Institute of Child Health and Human Development, National Institutes of Health , Eunice Kennedy Shriver , Bethesda, MD 20892 , USA

5. Center for Immuno-Oncology, Center for Cancer Research, National Cancer Institute, National Institutes of Health , Bethesda, MD 20892, USA

6. Neurosurgery Unit for Pituitary and Inheritable Diseases, National Institute of Neurological Disorders and Stroke, National Institutes of Health , Bethesda, MD 20892 , USA

7. Laboratory of Pathology, Center for Cancer Research, National Institutes of Health , Bethesda, MD 20892 , USA

8. Unit on Hypothalamic and Pituitary Disorders , Eunice Kennedy Shriver , Bethesda, MD 20892 , USA

Abstract

Abstract Context Spatial transcriptomic (ST) analysis of tumors provides a novel approach to studying gene expression along with the localization of tumor cells in their environment to uncover spatial interactions. Design We present ST analysis of corticotroph pituitary neuroendocrine tumors (PitNETs) from formalin-fixed, paraffin-embedded tissues. ST data were compared to immunohistochemistry results. Gene expression profiles were reviewed for cluster annotations, and differentially expressed genes were used for pathway analysis. Results Seven tumors were used for ST analysis. In situ annotation of tumor tissue was inferred from the gene expression profiles and was in concordance with the annotation made by a pathologist. Furthermore, relative gene expression in the tumor corresponded to common protein staining used in the evaluation of PitNETs, such as reticulin and Ki-67 index. Finally, we identified intratumor heterogeneity; clusters within the same tumor may present with different transcriptomic profiles, unveiling potential intratumor cell variability. Conclusion Together, our results provide the first attempt to clarify the spatial cell profile in PitNETs.

Funder

Intramural Research Program

National Institute of Child Health and Human Development

National Institutes of Health

Publisher

The Endocrine Society

Cited by 1 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. scRNA sequencing technology for PitNET studies;Frontiers in Endocrinology;2024-07-24

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