Table 1 Properties of the examined cell lines, TTFields treatment conditions, cellular cytotoxic response to TTFields, and the different transcriptomics methods employed for each dataset.

From: The transcriptomic fingerprint of cancer response to Tumor Treating Fields (TTFields)

Tumor type (abbreviation)

Cell line

Tumor origin

Donor sex

Growth mode

Doubling time [h]

TTFields treatment

Transcriptomics method

Ref

Frequency [kHz]

Intensity [V/cm RMS]

Duration [h]

Cell count [% of control]

24  h

48 h

Gastric cancer (GasC)

AGS

Primary

Female

Adherent

32

150

1.7

24, 48

74

30

PolyA RNA-seq with Unique Molecular Identifiers (UMI)

b

KATOIII

Metastatic

Male

Adherent

27

85

61

Pancreatic cancer (PanC)

AsPC1

Primary

Female

Adherent

33

150

79

62

BxPC3

Metastatic

Female

Adherent

45

72

49

Ovarian cancer (OvaC)

OVCAR3

Metastatic

Female

Adherent

54

200

64

41

Non-small cell lung carcinoma (NSCLC)

A549

Primary

Male

Adherent

22

150 a

1.5

12, 24, 48

88

47

Illumina Whole Genome HumanWG6 v4 Expression BeadChips

[18]

H1299

Metastatic

Male

Adherent

20

83

75

H157

N/A

Male

Adherent

36

96

33

H1650

Metastatic

Male

Adherent

26

95

84

HCC4006

Metastatic

Male

Adherent

34

106

87

Pleural Mesothelioma (Meso)

CD473

Primary

Male

Adherent

42

150

1.1

8, 24, 48

64

42

Whole RNA-seq

[30]

CD60

Primary

Female

Adherent

44

73

73

Glioblastoma (GBM)

GBM1

Primary

Male

Neurospheres

62

200

1.7

48

N/A

84

PolyA RNA-seq

c

JHH520

Primary

Female

Neurospheres

56

N/A

71

NCH644

Primary

Female

Neurospheres

102

N/A

73

SF188

Primary

Male

Neurospheres

37

N/A

75

  1. aNot all were treated at the same frequency, specific details may be found in the original publication of the datasets.
  2. bConducted by Novocure LTD, Haifa, Israel.
  3. cConducted by Renfei Du and Ulf Kahlert.