4.7 Article

Evaluation of EpCAM-specific exosomal lncRNAs as potential diagnostic biomarkers for lung cancer using droplet digital PCR

期刊

JOURNAL OF MOLECULAR MEDICINE-JMM
卷 100, 期 1, 页码 87-100

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00109-021-02145-4

关键词

EpCAM-specific exosomes; Lung cancer; Diagnosis; Lung adenocarcinoma; Squamous cell lung cancer; Digital polymerase chain reaction

资金

  1. National Natural Science Foundation of China [81902146]
  2. Natural Science Foundation of Zhejiang Province [LQ18H200001]
  3. Program of Xinmiao (Potential) Talents in Zhejiang Province [2020R405041, 2021R405044]
  4. Research Project in Ningbo University [JYXMXZD2021031, XYL20028]
  5. Research Project of Education Science in Ningbo City [2020YGH007]
  6. K.C.Wong Magna Fund in Ningbo University

向作者/读者索取更多资源

This study demonstrates the potential diagnostic value of EpCAM-specific exosomal lncRNAs RP11-77G23.5 and PHEX-AS1 for lung cancer. EpCAM-positive exosomes in serum were found to promote lung cancer development in vitro and in vivo. RP11-77G23.5 showed the ability to subtype LUAC and LUSC, while PHEX-AS1 was associated with lung cancer progression.
Accumulating evidence demonstrated that long non-coding RNAs (lncRNAs) derived from exosomes had the potential to be diagnostic markers for lung cancer. However, the diagnostic value of lncRNAs from epithelial cell adhesion molecule (EpCAM)-positive exosomes remains unclear. In the study, serum EpCAM-positive exosomes were isolated with magnetic beads, and their role in lung cancer was investigated in vitro and in vivo. The copy numbers of lncRNAs RP11-77G23.5 and PHEX-AS1 in EpCAM-specific exosomes were quantified by droplet digital PCR (ddPCR). The diagnostic value of RP11-77G23.5 and PHEX-AS1 was tested in the training cohort and verified in the validation cohort. We found that EpCAM-specific exosomes could promote lung cancer development in vitro and in vivo. RP11-77G23.5 and PHEX-AS1 were significantly elevated in EpCAM-specific exosomes from lung cancer patients and could distinguish malignant from benign lung tumors. The amounts of RP11-77G23.5 were statistically higher in the subtype of lung adenocarcinoma (LUAC) than that of lung squamous cell carcinoma (LUSC), showing its capability to subtype LUAC and LUSC, while PHEX-AS1 exhibited distinct expression signatures between lower and higher tumor stages, and without and with distant metastasis, indicating its association with lung cancer progression. In conclusion, the EpCAM-specific exosomal lncRNAs RP11-77G23.5 and PHEX-AS1 may be promising diagnostic biomarkers for lung cancer. Key messages Serum EpCAM-positive exosomes promote lung cancer development in vitro and in vivo. Two EpCAM-specific exosomal lncRNAs can be simultaneously detected by RT-ddPCR. EpCAM-specific exosomal RP11-77G23.5 has the potential to subtype LUAC and LUSC. EpCAM-specific exosomal PHEX-AS1 is associated with lung cancer progression.

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