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The prevalence of HLA-I LOH in Chinese pan-cancer patients and genomic features of patients harboring HLA-I LOH
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Loss of heterozygosity in HLA-I (HLA-I LOH) may facilitate immune
evasion. However, the large population study of HLA-I LOH in Chinese
pan-cancer patients remains to be explored. In this study, analysis was
performed in 1504 advanced pan-cancer patients and 134 early-stage NSCLC
patients using a 1021-gene panel. The consistency between the 1021-gene
panel and whole-exome sequencing (WES) was evaluated in 45 samples,
where concordant results were obtained in 95.6% (43/45) of the samples.
Analytical results revealed that the prevalence of HLA-I LOH presents
considerable differences across cancer types. HLA-I LOH was relevant to
genomic instability, reflected in higher tumor mutation burden (TMB)
level. The incidence of HLA-I LOH in MSS samples was significantly
higher than that in MSI-H samples. The alteration frequencies of p53
pathway, RTK/RAS pathway, Notch pathway, Hippo pathway, and Nrf2 pathway
in HLA-I LOH group were significantly higher than that in HLA-I stable
group (p<0.0001, p<0.0001, p=0.032, p=0.013,
p=0.003, respectively). In DNA damage response (DDR) pathways,
alterations in CPF pathway and FA pathway are enriched in HLA-I LOH
group (p<0.0001, p=0.023, respectively). Besides, HLA-I LOH
was accompanied by higher mutation rates of several tumor suppressors,
including TP53 and LRP1B. These results may shed light on follow-up
research.
Title: The prevalence of HLA-I LOH in Chinese pan-cancer patients and genomic features of patients harboring HLA-I LOH
Description:
Loss of heterozygosity in HLA-I (HLA-I LOH) may facilitate immune
evasion.
However, the large population study of HLA-I LOH in Chinese
pan-cancer patients remains to be explored.
In this study, analysis was
performed in 1504 advanced pan-cancer patients and 134 early-stage NSCLC
patients using a 1021-gene panel.
The consistency between the 1021-gene
panel and whole-exome sequencing (WES) was evaluated in 45 samples,
where concordant results were obtained in 95.
6% (43/45) of the samples.
Analytical results revealed that the prevalence of HLA-I LOH presents
considerable differences across cancer types.
HLA-I LOH was relevant to
genomic instability, reflected in higher tumor mutation burden (TMB)
level.
The incidence of HLA-I LOH in MSS samples was significantly
higher than that in MSI-H samples.
The alteration frequencies of p53
pathway, RTK/RAS pathway, Notch pathway, Hippo pathway, and Nrf2 pathway
in HLA-I LOH group were significantly higher than that in HLA-I stable
group (p<0.
0001, p<0.
0001, p=0.
032, p=0.
013,
p=0.
003, respectively).
In DNA damage response (DDR) pathways,
alterations in CPF pathway and FA pathway are enriched in HLA-I LOH
group (p<0.
0001, p=0.
023, respectively).
Besides, HLA-I LOH
was accompanied by higher mutation rates of several tumor suppressors,
including TP53 and LRP1B.
These results may shed light on follow-up
research.
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