Decoding Chemotherapy Resistance of Undifferentiated Pleomorphic Sarcoma at the Single Cell Resolution: A Case Report

被引:0
作者
Fetisov, Timur I. [1 ,2 ]
Menyailo, Maxim E. [1 ,3 ]
Ikonnikov, Alexander V. [1 ]
Khozyainova, Anna A. [1 ,3 ]
Tararykova, Anastasia A. [1 ,2 ]
Kopantseva, Elena E. [1 ]
Korobeynikova, Anastasia A. [1 ,3 ]
Senchenko, Maria A. [1 ,2 ]
Bokova, Ustinia A. [1 ,3 ]
Kirsanov, Kirill I. [1 ,2 ]
Yakubovskaya, Marianna G. [1 ,2 ]
Denisov, Evgeny V. [1 ,3 ]
机构
[1] RUDN Univ, Peoples Friendship Univ Russia, Res Inst Mol & Cellular Med, Moscow 115093, Russia
[2] NN Blokhin Natl Med Res Ctr Oncol, Moscow 115478, Russia
[3] Russian Acad Sci, Canc Res Inst, Tomsk Natl Res Med Ctr, Tomsk 634009, Russia
基金
俄罗斯科学基金会;
关键词
chemotherapy; resistance; undifferentiated pleomorphic sarcoma; soft tissue sarcoma; recurrence; single cell RNA sequencing; bioinformatics; transcriptome; TUMOR-ASSOCIATED MACROPHAGES;
D O I
10.3390/jcm13237176
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Undifferentiated pleomorphic sarcoma (UPS) is a highly malignant mesenchymal tumor that ranks as one of the most common types of soft tissue sarcoma. Even though chemotherapy increases the 5-year survival rate in UPS, high tumor heterogeneity frequently leads to chemotherapy resistance and consequently to recurrences. In this study, we characterized the cell composition and the transcriptional profile of UPS with resistance to chemotherapy at the single cell resolution. Methods: A 58-year-old woman was diagnosed with a 13.6 x 9.3 x 6.0 cm multi-nodular tumor with heterogeneous cysto-solid structure at the level of the distal metadiaphysis of the left thigh during magnetic resonance tomography. Morphological and immunohistochemical analysis led to the diagnosis of high-grade (G3) UPS. Neoadjuvant chemotherapy, surgery (negative resection margins), and adjuvant chemotherapy were conducted, but tumor recurrence developed. The UPS sample was used to perform single-cell RNA sequencing by chromium-fixed RNA profiling. Results: Four subpopulations of tumor cells and seven subpopulations of tumor microenvironment (TME) have been identified in UPS. The expression of chemoresistance genes has been detected, including KLF4 (doxorubicin and ifosfamide), ULK1, LUM, GPNMB, and CAVIN1 (doxorubicin), and AHNAK2 (gemcitabine) in tumor cells and ETS1 (gemcitabine) in TME. Conclusions: This study provides the first description of the single-cell transcriptome of UPS with resistance to two lines of chemotherapy, showcasing the gene expression in subpopulations of tumor cells and TME, which may be potential markers for personalized cancer therapy.
引用
收藏
页数:14
相关论文
共 55 条
  • [1] Berlow Noah E., 2020, Sarcoma, V2020, P6312480, DOI 10.1155/2020/6312480
  • [2] HSP90 inhibitors induce GPNMB cell-surface expression by modulating lysosomal positioning and sensitize breast cancer cells to glembatumumab vedotin
    Biondini, Marco
    Kiepas, Alex
    El-Houjeiri, Leeanna
    Nis, Matthew G. An
    Hsu, Brian E.
    Fortier, Anne-Marie
    Morin, Genevieve
    Martina, Jose A.
    Sirois, Isabelle
    Aguilar-Mahecha, Adriana
    Gruosso, Tina
    McGuirk, Shawn
    Rose, April A. N.
    Tokat, Unal M.
    Johnson, Radia M.
    Sahin, Ozgur
    Bareke, Eric
    St-Pierre, Julie
    Park, Morag
    Basik, Mark
    Majewski, Jacek
    Puertollano, Rosa
    Pause, Arnim
    Huang, Sidong
    Keler, Tibor
    Siegel, Peter M.
    [J]. ONCOGENE, 2022, 41 (12) : 1701 - 1717
  • [3] Undifferentiated Pleomorphic Sarcoma: Long-Term Follow-Up from a Large Institution
    Chen, Shiqi
    Huang, Wending
    Luo, Peng
    Cai, Weiluo
    Yang, Lingge
    Sun, Zhengwang
    Zheng, Biqiang
    Yan, Wangjun
    Wang, Chunmeng
    [J]. CANCER MANAGEMENT AND RESEARCH, 2019, 11 : 10001 - 10009
  • [4] ECM2, a prognostic biomarker for lower grade glioma, serves as a potential novel target for immunotherapy
    Cheng, Xingbo
    Liu, Zhendong
    Liang, Wenjia
    Zhu, Qingyun
    Wang, Chao
    Wang, Hongbo
    Zhang, Jiangfen
    Li, Pengxu
    Gao, Yanzheng
    [J]. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2023, 158
  • [5] Cancer-associated fibroblast classification in single-cell and spatial proteomics data
    Cords, Lena
    Tietscher, Sandra
    Anzeneder, Tobias
    Langwieder, Claus
    Rees, Martin
    de Souza, Natalie
    Bodenmiller, Bernd
    [J]. NATURE COMMUNICATIONS, 2023, 14 (01)
  • [6] A variational algorithm to detect the clonal copy number substructure of tumors from scRNA-seq data
    De Falco, Antonio
    Caruso, Francesca
    Su, Xiao-Dong
    Iavarone, Antonio
    Ceccarelli, Michele
    [J]. NATURE COMMUNICATIONS, 2023, 14 (01)
  • [7] Primary Culture of Undifferentiated Pleomorphic Sarcoma: Molecular Characterization and Response to Anticancer Agents
    De Vita, Alessandro
    Recine, Federica
    Mercatali, Laura
    Miserocchi, Giacomo
    Spadazzi, Chiara
    Liverani, Chiara
    Bongiovanni, Alberto
    Pieri, Federica
    Casadei, Roberto
    Riva, Nada
    Fausti, Valentina
    Amadori, Dino
    Ibrahim, Toni
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (12)
  • [8] Heterogeneity of Soft Tissue Sarcomas and Its Implications in Targeted Therapy
    Du, Xin-Hui
    Wei, Hua
    Zhang, Peng
    Yao, Wei-Tao
    Cai, Qi-Qing
    [J]. FRONTIERS IN ONCOLOGY, 2020, 10
  • [9] Perspectives of Cell Sensitivity/Resistance Assay in Soft Tissue Sarcomas Chemotherapy
    Fetisov, Timur I.
    Khazanova, Sofya A.
    Shtompel, Polina A.
    Trapeznikova, Ekaterina S.
    Zinovieva, Victoria Y.
    Marshall, Valeria I.
    Lovenger, Anastasia A.
    Rogozhin, Dmitriy V.
    Anastasia, Tararykova A.
    Bokhyan, Beniamin Yu.
    Belitsky, Gennady A.
    Yakubovskaya, Marianna G.
    Kirsanov, Kirill I.
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (15)
  • [10] MAST: a flexible statistical framework for assessing transcriptional changes and characterizing heterogeneity in single-cell RNA sequencing data
    Finak, Greg
    McDavid, Andrew
    Yajima, Masanao
    Deng, Jingyuan
    Gersuk, Vivian
    Shalek, Alex K.
    Slichter, Chloe K.
    Miller, Hannah W.
    McElrath, M. Juliana
    Prlic, Martin
    Linsley, Peter S.
    Gottardo, Raphael
    [J]. GENOME BIOLOGY, 2015, 16