International Journal of Engineering Technology and Management Sciences

2023, Volume 7 Issue 2

A SURVEY ON CANCER SUBTYPING BASED ON DEEP LEARNING USING PAN-CANCER AND MULTIOMIC DATA

AUTHOR(S)

S.Keerthana, K.Shanmugapriya

DOI: https://doi.org/10.46647/ijetms.2023.v07i02.073

ABSTRACT
Tumor subclasses with clinical implications are identified by breast cancer gene expression patterns. In this study, ROBERT TIBSHIRANI et al. make a suggestion. Based on changes in gene expression, the tumours were divided into three groups: basal epithelial-like, ERBB2-overexpressing, and normal breast-like. Two separate gene sets, one representing a collection of 456 cDNA clones originally chosen to reflect intrinsic tumour features and the other being a gene set that was highly correlated with patient prognosis, were clustered to reveal that both groupings were quite robust. The basal-like subtype had a dismal prognosis, and the two oestrogen receptor-positive groups had significantly different outcomes, according to survival studies on a sub cohort of patients. In this study, three fibroadenomas and 78 breast carcinomas were examined. This collection comprises of 40 tumours that have already been studied and characterised. A total of 85 tissue samples from 84 individuals were examined.

Page No: 643 - 655

References:

[1] T. Srlie et al., "Gene expression patterns of breast carcinomas define tumour subtypes with clinical implications," Proc. Nat. Acad. Sci. United States, vol. 98, no. 19, pp. 10869-10874, 2001.
[2] A. F. Vieira and F. Vieira Schmitt, "An update on multigene predictive testing for breast cancer-emergent clinical signs," Front. Med., vol. 5, no. 248, 2018.
[3] J. Parker et al., "Supervised risk predictor of breast cancer based on intrinsic subtypes," J. Clin. Oncology, vol. 27, pp. 1160-1167, 2009.
[4] B. Wallden et al., "Development and validation of the PAM50-based prosigna breast cancer gene signature test," BMC Med. Vol. 1 Genomics Art. no. 54, 8, no. 1, 2015.
[5] Cancer Genome Atlas Network et al., Nature, vol. 490, no. 7418 (2012), pp. 61-70.
[6] A. M. Sabhiya, B. Showkat, and H. "Micrornas and its Emerging Role as Breast Cancer Diagnostic Marker- A Review," Tehseen, Advances Biomarker Sci. Applied Technology, vol. 1, no. 1, 2019, pp. 1-8.
[7] F. L. S. Oliveira, C. Petitjean, and A. Spanhol, "Breast cancer histopathology picture classification using convolutional neural networks," by Heutte, published in Neural Networks, 2016. [8] R. S. Goodison, S. Chen, and Y. Sun, "Deep-learning approach for cancer subtype detection utilising
[9] S. I. Saha, S. S. Chakraborty, and D. Rakshit Plewczyski, "Deep learning for integrated analysis of multi-omics data from breast cancer subtypes," IEEE Region 10 Conference Proceedings, 2018, pp. 1917-1922.
[10] M. G. Wicaksono, R. Karim, I. G. Costa, S. Decker, and O. Beyan, "Multimodal genomics-based prognostic subtypes and breast cancer survival prediction," IEEE Access, vol. 7, pp. 133850-133864, 2019.
[11] Braschi, B. B., Gray, K. A., Seal, R. L., Tweedie, and E. Yates A. Bruford, Nucleic Acids Res., vol. 45, no. D1, pp. D619-D625, 2017. "Genenames.org: The HGNC and VGNC resources in 2017," Nucleic Acids Res., vol. 45, no. D1, pp. D619-D625, 2017.
[12] Hinton, N. G., Krizhevsky, Sutskever, and R. Srivastava Salakhutdinov, J. Mach., "Dropout: A Simple Way to Prevent Neural Network Overfitting," Jan. 2014, Learn. Research, vol. 15, pages 1929-1958.
[13] D. M. Kingma and P. Kingma, "Auto-encoding variational bayes," Welling, Proc. 2nd International Conference on Learning Representations, pp. 1-14, arXiv:1312.6114, 2014.
[14] C. Doersch's "Tutorial on Variational Autoencoders," arXiv:1606.05908.
[15] K. H. Sohn, X. Yan, and Sohn Lee, "Learning structured output representation using deep conditional generative models," Proceedings of the National Academy of Sciences, vol. 28th International Conference on Artificial Neural Processes and Systems, pp. 3483-3491, 2015.
[16] D. Zhang, Y. N. Dauphin, and H. M. Cisse Lopez-Paz, "Mixup: Beyond Empirical Risk Minimization," Proc. 6th International Conf. Learn. Representations, arXiv:1710.09412 (2018, pp. 1-13).
[17]  M. S. Singh, Ribeiro, and C. "How can I believe you?" Guestrin inquires. ": Explaining any classifier's predictions," ACM SIGKDD 22nd International Conference on Knowledge Discovery and Data Mining, pp. 1135-1144, 2016.
[18] Nucleic Acids Res., vol. 45, no. D1, pp. D877-D887, 2016. N. Rappaport et al. "MalaCards: A combined human illness database with diverse clinical and genetic annotation and organised search."
[19] Nucleic Acids Res., vol. 46, no. D1, pp. D296-D302, 2018. C.-H. MiRTarBase update 2018: A database of experimentally confirmed microRNA-target interactions. Chou and colleagues
[20] A. Hoadley et al., "Multiplatform investigation of 12 cancer types shows molecular classification inside and across tissues of origin," Cell, vol. 158, no. 4, pp. 929-944,2014


How to Cite This Article:
S.Keerthana, K.Shanmugapriya . A SURVEY ON CANCER SUBTYPING BASED ON DEEP LEARNING USING PAN-CANCER AND MULTIOMIC DATA . ijetms;7(2):643-655. DOI: 10.46647/ijetms.2023.v07i02.073