journal article·2025-04-23

Programmable Loading of a Multivalent LRPPRC Aptamer onto a Rectangular DNA Tile Inhibits the Proliferation of Lung Adenocarcinoma Cells

Xinna Zhang, Yunben Yang, Zhan Tian, Ziyan Du, Wei Zhou, Ting Fu, Linfeng Zheng, Cong Luo, Ruizi Peng, Weihong Tan

ACS Applied Materials & Interfaces· Volume 17· Issue 16
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Abstract

Since cancer biomarkers for lung adenocarcinoma can lead to early intervention and treatment, they have been the focus of much research attention. DNA aptamers, which are functional oligonucleotides, exhibit high specificity and binding affinity to different types of cancer biomarkers. Through DNA aptamer screening, a leucine-rich PPR-motif-containing protein (LRPPRC) was discovered as a potential biomarker for lung adenocarcinoma therapeutics. It is an RNA-binding protein that helps in regulating post-transcriptional gene expression in mitochondria. Interestingly, the first LRPPRC-targeted small-molecule drug showed significant antitumor effects. Apart from biomarker discovery, DNA aptamers have also shown promise in cancer therapeutics, but challenges in the programmable delivery of aptamers have limited applications. Herein, we have addressed these challenges in two steps. First, after obtaining purified protein LRPPRC, we verified aptamer R14 as its high-affinity binding ligand. Second, for programmable delivery, a rectangular DNA tile (RDT) was constructed to improve cellular internalization. In particular, DNA handles on the surface of this DNA nanostructure serve as overhangs for loading multivalent R14, and both A549 and PC9 cells treated with R14-RDT targeted to LRPPRC showed significant inhibition of cancer cell proliferation. We then investigated the molecular mechanism(s) underlying the interaction between multivalent aptamer R14 loaded on an RDT and its cognate target protein such that the result is inhibition of cancer cell proliferation. Based on our findings, we hypothesized that R14-RDT-LRPPRC interaction triggers significant gene transcription and RNA processing events that result in inhibiting mitochondria-related genes and RNA transcriptional processing, while causing an immune inflammatory response that ultimately leads to the inhibition of cancer cell proliferation. Therefore, this research offers an instructive paradigm for programmable loading of a multivalent aptamer onto a two-dimensional DNA nanostructure to improve targeted cancer therapeutics through intervening with the cell's transcriptome.
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Research context

OpenAlex topics: Advanced biosensing and bioanalysis techniques · RNA Interference and Gene Delivery · DNA and Nucleic Acid Chemistry

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Life Sciences, Faculty of Medicine

Tianjin University

Zhejiang Cancer Hospital, Key Laboratory of Zhejiang Province for Aptamers and Theranostics

Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences

Beijing National Research Center for Molecular Sciences

Institute of Chemistry, Chinese Academy of Science

Molecular Science and Biomedicine Laboratory (MBL), State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, College of Biology, Aptamer Engineering Center of Hunan Province

Hunan University

Funding

National Natural Science Foundation of China · Natural Science Foundation of Zhejiang Province · Zhejiang Provincial Jianbing Lingyan Key Research and Development Project · Zhejiang Basic Public Welfare Research Program · Zhejiang Leading Innovation and Entrepreneurship Team

References (43)

Show source-provided references
1. 10.1038/nature1338510.1038/nature13385 ↗
2. 10.1038/nm73310.1038/nm733 ↗
3. 10.3322/caac.2182010.3322/caac.21820 ↗
4. 10.1126/science.109931410.1126/science.1099314 ↗
5. 10.1056/NEJMoa121488610.1056/NEJMoa1214886 ↗
6. 10.1158/1078-0432.CCR-18-016310.1158/1078-0432.CCR-18-0163 ↗
7. 10.6004/jnccn.2204.002310.6004/jnccn.2204.0023 ↗
8. 10.1038/346818a010.1038/346818a0 ↗
9. 10.1038/nprot.2010.6610.1038/nprot.2010.66 ↗
10. 10.1073/pnas.060261510310.1073/pnas.0602615103 ↗
11. 10.1126/science.220012110.1126/science.2200121 ↗
12. 10.1021/acsami.0c1564410.1021/acsami.0c15644 ↗
13. 10.1021/acsami.0c1956210.1021/acsami.0c19562 ↗
14. 10.1186/s40824-023-00365-y10.1186/s40824-023-00365-y ↗
15. Zhang X. · Prog. Biochem Biophys · 2023 · 50 · 2037
16. 10.1021/jacs.9b0877710.1021/jacs.9b08777 ↗
17. 10.1038/emboj.2011.39210.1038/emboj.2011.392 ↗
18. 10.1038/s41467-017-01221-z10.1038/s41467-017-01221-z ↗
19. 10.1016/j.ijbiomac.2024.13682010.1016/j.ijbiomac.2024.136820 ↗
20. 10.1038/s41594-024-01365-910.1038/s41594-024-01365-9 ↗
21. 10.1021/accountsmr.3c0024910.1021/accountsmr.3c00249 ↗
22. 10.1021/jacs.3c0084110.1021/jacs.3c00841 ↗
23. 10.1021/acsami.3c1806810.1021/acsami.3c18068 ↗
24. 10.1021/acs.chemrev.7b0066310.1021/acs.chemrev.7b00663 ↗
25. 10.1002/anie.20221533210.1002/anie.202215332 ↗
26. 10.1002/anie.20170948510.1002/anie.201709485 ↗
27. 10.3389/fgene.2021.81767210.3389/fgene.2021.817672 ↗
28. 10.1021/acscentsci.1c0109010.1021/acscentsci.1c01090 ↗
29. 10.1038/s41467-023-39854-y10.1038/s41467-023-39854-y ↗
30. 10.1016/j.omto.2021.06.00910.1016/j.omto.2021.06.009 ↗
31. 10.1111/febs.1656710.1111/febs.16567 ↗
32. 10.1371/journal.pgen.100542310.1371/journal.pgen.1005423 ↗
33. 10.1038/s41419-021-04238-x10.1038/s41419-021-04238-x ↗
34. 10.1016/j.bbagrm.2011.10.00710.1016/j.bbagrm.2011.10.007 ↗
35. 10.1038/s41598-021-84787-510.1038/s41598-021-84787-5 ↗
36. 10.1021/acsami.3c1672310.1021/acsami.3c16723 ↗
37. 10.2174/011566523227952824011507535210.2174/0115665232279528240115075352 ↗
38. 10.1038/s41573-021-00371-610.1038/s41573-021-00371-6 ↗
39. 10.1196/annals.1348.06210.1196/annals.1348.062 ↗
40. 10.1038/s41433-023-02548-210.1038/s41433-023-02548-2 ↗
41. 10.1038/s41467-022-31997-810.1038/s41467-022-31997-8 ↗
42. 10.1021/acsami.4c0925210.1021/acsami.4c09252 ↗
43. 10.1016/j.jsb.2012.09.00610.1016/j.jsb.2012.09.006 ↗