2022
DOI: 10.1007/s11912-022-01316-x
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Small Cell and Other Rare Histologic Types of Cervical Cancer

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Cited by 4 publications
(3 citation statements)
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“…Understanding the molecular classifications of RCs could provide directions for successful targeted therapies. The common treatment options for male and female RCs are chemotherapy, immunotherapy, and radiotherapy [28][29][30][31]. PCa is classified into several subtypes with different clinicopathological features based on eight molecular classifications: tomlins, the cancer genome atlas (TCGA), prostate cancer 14-pathway (PCS), 50-gene signature (PAM50), bone-metastatic, epithelial, immune, and multi-omics [28].…”
Section: Introductionmentioning
confidence: 99%
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“…Understanding the molecular classifications of RCs could provide directions for successful targeted therapies. The common treatment options for male and female RCs are chemotherapy, immunotherapy, and radiotherapy [28][29][30][31]. PCa is classified into several subtypes with different clinicopathological features based on eight molecular classifications: tomlins, the cancer genome atlas (TCGA), prostate cancer 14-pathway (PCS), 50-gene signature (PAM50), bone-metastatic, epithelial, immune, and multi-omics [28].…”
Section: Introductionmentioning
confidence: 99%
“…SCCC and gastric-type adenocarcinoma are characterized by high genetic alterations, including mutations in TP53, Kirsten rat sarcoma viral oncogene homologue (KRAS), phosphatase and tensin homologue (PTEN), AT-rich interaction domain 1A (ARID1A), and p110alpha catalytic subunit of PI3K (PIK3CA). Immune checkpoint inhibitors such as poly(ADP-ribose) polymerase (PARP) inhibitors have shown the potential to inhibit PARP expression in SCCC cells [31].…”
Section: Introductionmentioning
confidence: 99%
“…Small-cell neuroendocrine carcinoma of the cervix (SCNCC) is a rare pathological type of cervix neoplasm with highly aggressive biological behaviors and poorer prognosis than the most common counterpart with squamous carcinoma [1,2]. Several different names were used in the past and now it is considered a high-grade malignancy classified as neuroendocrine carcinoma along with carcinoid tumor, atypical carcinoid tumor, and large cell neuroendocrine tumor [3].…”
mentioning
confidence: 99%