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Table 1 The genes with high frequency in 13 “sKLD-signaling genes” groups in the critical stage (stage IIA) for LUSC

From: Identifying critical state of complex diseases by single-sample Kullback–Leibler divergence

Gene

Frequency

Location

Family*

Relation with cancer progression

BIRC5

13

Cytoplasm

other

The miR-195 axis regulates lung squamous cell carcinoma (LUSC) progression through BIRC [39].

CCNA2

13

Nucleus

other

CCNA2 promotes invasion and migration of non-small cell lung cancer cells through integrin αvβ3 signaling

pathway [40].

CDC6

13

Nucleus

other

miR-26a/b inhibits directly migration, invasion, and proliferation of lung cancer cells by targeting CDC6 [41].

CKS1B

13

Other

kinase

CKS1B is a lung cancer-related gene, knockdown of which can result in a significant decrease in lung cancer cell proliferation, invasion and migration [42].

E2F8

13

Nucleus

transcription regulator

Depletion of E2F8 inhibits cell proliferation and tumor growth in lung cancer, thus E2F8 can be considered as a novel therapeutic target for lung cancer [43].

FOXM1

13

Nucleus

transcription regulator

Knockdown of FOXM1 inhibits the cell proliferation

in LUSC [44].

ITPKA

13

Cytoplasm

kinase

ITPKA serves as an early diagnostic marker in lung cancer, whose overexpression promotes tumorigenesis [45].

MCM2

13

Nucleus

enzyme

MCM2 regulates proliferation and cell cycle in lung squamous cell carcinoma, whose overexpressed protein is obviously associated with malign differentiated degree and lymph node metastasis [46].