Improved experiment
The introduction of our experiment
Our improved experiment is based upon the topic of YiYe-Wuhan iGEM 2024. The project aims at constructing
novel bio-therapeutics through siRNA delivery systems for improving treatments of colorectal cancer
(CRC)(Huang et al., 2022; Lee et al., 2016).
The Hippo pathway is a key regulatory pathway in tumorigenesis, it regulates genes that are closely linked
to cell proliferation and apoptosis, with TEAD1~4 being a core transcription factor that promotes the growth
and spread of CRC cancer cells. Moreover, TEAD4 is upregulated in cancerous tissues compared to
paracancerous tissues(Fu et al., 2022; Guo et al., 2022). Therefore, interfering with the function of TEAD4
is considered an effective strategy to inhibit tumor growth.
In our project, we have constructed two shRNA plasmids to inhibit the expression of TEAD4(Kang et al.,
2018). From our engineering success section, we have concluded that shRNA could indeed decreased the
proliferation and migration abilities and increased the ROS level in the CRC cell. For extensions on this
project, we propose two other approaches that could possibly have better effects on the same compared
categories. The former one being the direct transfection of siRNA into cancer cells. The latter one being
the alteration of nuclear translocation of TEAD4, namely NLS (nuclear location sequence) (Figure 1). All
experiments are done vitro with the transfection of target gene sequence.
Figure 1 Schematic diagram of three different methods of improving treatments of colorectal cancer
targeting at TEAD4
shRNA method is described in detailed in our engineering success method; siRNA method is directly delivered
the siRNA oligo into CRCs; NLS method means destroyed the protein nuclear location ability by deleted the
105aa to 109aa of TEAD4, therefore, TEAD4 unable to get into the nuclear and function as transcription
factor.
Design and Synthesis of siRNA oligo
siRNA wizard software (Invivo gen) (https://www.invivogen.com/sirnawizard/) is used in the design process of
siRNA sequence, there are built in algorithms that identify and lowers the off-target possibility of the
siRNA. Due to the complex relationship between the pattern of the sequence and the off-target possibility,
multiple siRNA sequence is given to us, and we chose two with the least off target possibility. The
synthesis of the designed siRNA is done by Tsingke Biotechnology, where we send them the designed sequence
and they generate it for us. shRNA follows the same design process but requires a designed hairpin structure
that connects the sense and anti-sense strand.
Construction of nuclear localization signal (NLS)-deletion TEAD4
(PMMP-TEAD4 △105-109)
TEAD4 isoform 1 were cloned by RT-PCR using RNA isolated from cells with primers (GCGGACTCCTTGGAACTGGCTTAG)
and (CATCTTGGGTTTATTTG
GGGTTGG) of TEAD4, respectively. The RT-PCR products were cloned to pTOPO vector (Invitrogen) and then
subjected to DNA sequence analysis.
We predicted the potential nuclear localization sequence of TEAD4, LARRK (105-109), using the PSORTⅡ
software (https://psort.hgc.jp/).The forward and reverse primers of TEAD4-NLS were
CTCCAGCCACATCCAGGTG/GCTCGCGA- GATCCAGGC and GCCTGGATCTCGCGAGC/CACCTGGATGTGGCTGGAG, in which the
“ctggctcgtcgcaaa” sequence corresponding to putative nuclear localization signal LARRK (leu-105 to lys-109)
was deleted. The first-round PCRs were carried out with TEAD4 cDNA as a template, with primers of
EcorRI-TEAD4-F (5’-AACTCGAGTTGGAGGGCACGGCCGGCAC) and TEAD4-NLS-R, TEAD4-NLS-F and BamHI-TEAD4-R
(5’-AAGGATCCTCATTCTTTCACCAGCCTG), respectively. The two PCR products were used as template for the
second-round PCR with primers EcorRI-TEAD4-F and BamHI-TEAD4-R. The PCR product was sequenced and subcloned
to pMMPc vector which number in Addgene is 116920. This generated cDNA sequence was later inserted into CRC
cells.
Compared three methods on cell proliferation by CCK-8 experiment
Cell Counting Kit-8, is a pragmatic method used to examine the toxicity and proliferation ability of cells.
The deeper the color shown on the cell, the faster and more substantial the cell proliferates.
To further test the proliferation ability, SW480 cells were transfected with siRNA oligo, sh-TEAD4-1 plasmid
and NLS plasmid with different dosage (0 μg, 0.5μg, 1μg, 2μg) (Fig 2). We found that NLS method showed
better effect on inhibiting cell proliferation while siRNA displayed little effect on inhibiting cell
proliferation.
Figure 2 the proliferation changes after transfected with three different methods
(upper is the chromogenic reaction of CCK8 experiment in 96 well plate. Relative cell viability was
normalized by the control sh-TEAD4-1 group ***means p<0.01, ****means p<0.001 by Student’s
t-test significance, ns means none significance)
Compared three methods on cell migration by transwell experiment
Transwell experiment is a tool used to measure the migration ability of cells. There are three kinds of
plasmids/oligo that we infected into CRC cells, siRNA oligo, sh-TEAD4-1 plasmid and NLS plasmid,
respectively. Then we infect 0, 0.5µg, 1µg, 2µg of blank plasmid into the CRC cells. We also found that NLS
method showed remarkable effect on inhibiting cell migration while siRNA showed worse function on inhibiting
cell migration compared to our sh-TEAD4 method.
Figure 3 the migration ability detection after transfected with three different methods
(Representative images of the total view of the transwell were shown, sw480 cell were transfected
with PLKO.1 plasmid, sh-TEAD4-1 and sh-TEAD4-2 composite plasmid that could silence TEAD4 gene
expression, data were collected from 10 fields of three independent experiments)
Figure 4 the statistical diagram of migration ability detection
(***means p<0.01, ****means p<0.001 by Student’s t-test significance, ns means none
significance)
Compared three methods on cell migration of ROS level
The reactive oxygen species, ROS, is a kind of cell’s metabolic product generating by the metabolism of
oxygen. One main source of it is the substrate end of the inner mitochondrial membrane. As the metabolic
by-product, ROS is considered as the vicious biomacromolecule. The other main source is the nicotinamide
adenine dinucleotide phosphate (NADPH) oxidase, which is expressed on the plasma membrane. In the normal
condition, the amount of ROS stays in a low level. However, when the cell meets stimulus, the ROS level
would increase dramatically, exceeding the amount that the cell can process. This would lead to the
oxidative stress in the cell, causing the cell’s apoptosis. ROS level is an important marker of cellular
oxidative damage caused by normal physiological function and environmental factors. Therefore, it’s
necessary to measure the ROS level in our experiment.
In our experiment, we transfected the siRNA oligo, sh-TEAD4-1 plasmid and NLS plasmid into the SW480 cancer
cell, and we detected the ROS level in these cells. We found that NLS method showed better effect on
increasing cell ROS level while siRNA showed worse effect on increasing cell ROS level.
Figure 5 the ROS level detection after transfected with three different methods
(Representative images of the total view of the ROS were shown, sw480 cell were transfected with
PLKO.1 plasmid, sh-TEAD4-1 and sh-TEAD4-2 composite plasmid that could silence TEAD4 gene
expression. Data were collected from 10 fields of three independent experiments.)
Figure 6 the statistical diagram of ROS level detection
(***means p<0.01, ****means p<0.001 by Student’s t-test significance, ns means none
significance)
Figure 7 The summary diagram of the improvement experiment
Conclusion
From the data of previous results, we can conclude that NLS achieved the greatest outcomes for all of three
demonstrations, followed by shRNA, then siRNA (Figure 7). For analysis, siRNA achieved the worst results
because that isn't long lasting, its half-life is roughly 48 hours. Normally, RNA will be degraded by really
common enzymes, this leads to the loss of effectiveness for siRNA treatments. As an innovative method, NLS
achieved even better results, there are multiple approaches that could be thought of and tested because of
the complex structures of the hippo pathways. Cancer as a whole is a complex topic, and dealing it requires
a better understanding of it. Topics like prohibiting tumor microenvironment (TME) development and
metastatic cell regulations can be possible future directions. But more validation is needed for the sake of
safety and effectiveness of these types of innovative therapies.
Reference
Huang, C.Z., Zhou, Y., Tong, Q.S., Duan, Q.J., Zhang, Q., Du, J.Z., and Yao, X.Q. (2022). Precision
medicine-guided co-delivery of ASPN siRNA and oxaliplatin by nanoparticles to overcome chemoresistance of
colorectal cancer. Biomaterials 290, 121827.
Kang, W., Huang, T., Zhou, Y., Zhang, J., Lung, R.W.M., Tong, J.H.M., Chan, A.W.H., Zhang, B., Wong, C.C.,
Wu, F., et al. (2018). miR-375 is involved in Hippo pathway by targeting YAP1/TEAD4-CTGF axis in gastric
carcinogenesis. Cell Death Dis 9, 92.
Fu, M., Hu, Y., Lan, T., Guan, K.L., Luo, T., and Luo, M. (2022). The Hippo signalling pathway and its
implications in human health and diseases. Signal Transduct Target Ther 7, 376.
Guo, Y., Zhu, Z., Huang, Z., Cui, L., Yu, W., Hong, W., Zhou, Z., Du, P., and Liu, C.Y. (2022). CK2-induced
cooperation of HHEX with the YAP-TEAD4 complex promotes colorectal tumorigenesis. Nat Commun 13, 4995.
Lee, S.Y., Yang, C.Y., Peng, C.L., Wei, M.F., Chen, K.C., Yao, C.J., and Shieh, M.J. (2016). A theranostic
micelleplex co-delivering SN-38 and VEGF siRNA for colorectal cancer therapy. Biomaterials 86, 92-105.