Single-cell RNA sequencing highlights intratumor heterogeneity and intercellular network featured in adamantinomatous craniopharyngioma

Author:

Jiang Yu1ORCID,Yang Jinlong1ORCID,Liang Ruichao1ORCID,Zan Xin1ORCID,Fan Rangrang1ORCID,Shan Baoyin1,Liu Hao1ORCID,Li Li2ORCID,Wang Yue3ORCID,Wu Min4ORCID,Qi Xin1ORCID,Chen Hongxu1ORCID,Ren Qingqing1ORCID,Liu Zhiyong1,Wang Yuelong1,Zhang Jing1ORCID,Zhou Peizhi1ORCID,Li Qiang1ORCID,Tian Meng1ORCID,Yang Jinhao1ORCID,Wang Chaoyang1ORCID,Li Xueying1,Jiang Shu1ORCID,Zhou Liangxue1ORCID,Zhang Gao5ORCID,Chen Yaohui6ORCID,Xu Jianguo1ORCID

Affiliation:

1. Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu, 610041, China.

2. Institute of Clinical Pathology, West China Hospital, Sichuan University, Chengdu, 610041, China.

3. Department of Gastroenterology, Qilu Hospital of Shandong University, Jinan, 250000, China.

4. Huaxi MR Research Center (HMRRC), Department of Radiology, Functional and Molecular Imaging Key Laboratory of Sichuan Province, West China Hospital, Sichuan University, Chengdu, 610041, China.

5. Faculty of Dentistry, The University of Hong Kong, Sai Ying Pun, 999077, Hong Kong.

6. Department of Thoracic Surgery/Institute of Thoracic Oncology, West China Hospital, Sichuan University, Chengdu, 610041, China.

Abstract

Despite improvements in microscopically neurosurgical techniques made in recent years, the prognosis of adamantinomatous craniopharyngioma (ACP) is still unsatisfactory. Little is known about cellular atlas and biological features of ACP. Here, we carried out integrative analysis of 44,038 single-cell transcriptome profiles to characterize the landscape of intratumoral heterogeneity and tumor microenvironment (TME) in ACP. Four major neoplastic cell states with distinctive expression signatures were defined, which further revealed the histopathological features and elucidated unknown cellular atlas of ACP. Pseudotime analyses suggested potential evolutionary trajectories between specific neoplastic cell states. Notably, a distinct oligodendrocyte lineage was identified in ACP, which was associated with immunological infiltration and neural damage. In addition, we described a tumor-centric regulatory network based on intercellular communication in TME. Together, our findings represent a unique resource for deciphering tumor heterogeneity of ACP, which will improve clinical diagnosis and treatment strategies.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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